# geneInfo

ensembl_gene_id: ENSCAFG00845020527
chromosome_name: 32
gene_biotype: protein_coding
symbol: SMARCAD1
description:
  SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 


ensembl_gene_id: ENSCAFG00845027175
chromosome_name: 31
gene_biotype: protein_coding
symbol: GART
description:
  Phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase 


ensembl_gene_id: ENSCAFG00845021709
chromosome_name: 17
gene_biotype: protein_coding
symbol: MTHFD2
description:
  Methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase 


# pathwayInfo

id: 53
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C530698
name:
  Drug.CTD_v4_cfa_gskb_MESH:C530698_1-(2-(2-(3,4-dichlorophenyl)-4-(3,4,5-trimethoxybenzoyl)morpholin-2-yl)ethyl)spiro(benzo(c)thiophene-1(3H),4'-piperidine)-2-oxide

description:
  MESH:C530698 1-(2-(2-(3,4-dichlorophenyl)-4-(3,4,5-trimethoxybenzoyl)morpholin-2-yl)ethyl)spiro(benzo(c)thiophene-1(3H),4'-piperidine)-2-oxide


id: 55
n: 2
memo: https://ctdbase.org/detail.go?type=chem&acc=C569670
name:
  Drug.CTD_v4_cfa_gskb_MESH:C569670_1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-morpholinothieno(3,2-d)pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one

description:
  MESH:C569670 1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-morpholinothieno(3,2-d)pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one


id: 57
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C561237
name:
  Drug.CTD_v4_cfa_gskb_MESH:C561237_1-((4-cyano-4-pyridin-2-ylpiperidin-1-yl)methyl)-4-oxo-4H-quinolizine-3-carboxylic_acid

description:
  MESH:C561237 1-((4-cyano-4-pyridin-2-ylpiperidin-1-yl)methyl)-4-oxo-4H-quinolizine-3-carboxylic acid


id: 58
description: MESH:C525468 1-(5-(4-chlorophenyl)-4-(4-pyridinyl)-1H-pyrazol-3-yl)-4-methylpiperazine
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C525468
name:
  Drug.CTD_v4_cfa_gskb_MESH:C525468_1-(5-(4-chlorophenyl)-4-(4-pyridinyl)-1H-pyrazol-3-yl)-4-methylpiperazine


id: 63
description: MESH:C101670 2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea methanesulfonate
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C101670
name:
  Drug.CTD_v4_cfa_gskb_MESH:C101670_2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea_methanesulfonate


id: 68
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C477861
name:
  Drug.CTD_v4_cfa_gskb_MESH:C477861_(2-(5-amino-2-(4-fluorophenyl)-1,6-dihydro-6-oxo-1-pyrimidinyl)-N-(1-((5-methoxycarbonyl-2-benzoxazolyl)carbonyl)-2-phenylethyl)acetamide)

description:
  MESH:C477861 (2-(5-amino-2-(4-fluorophenyl)-1,6-dihydro-6-oxo-1-pyrimidinyl)-N-(1-((5-methoxycarbonyl-2-benzoxazolyl)carbonyl)-2-phenylethyl)acetamide)


id: 71
description: MESH:C511621 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amide
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C511621
name:
  Drug.CTD_v4_cfa_gskb_MESH:C511621_2-methyl-2H-pyrazole-3-carboxylic_acid_(2-methyl-4-o-tolylazophenyl)amide


id: 72
description: MESH:C054649 3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C054649
name:
  Drug.CTD_v4_cfa_gskb_MESH:C054649_3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol


id: 74
description: MESH:C482900 3-((3-trifluoromethyl)phenyl)-5-((3-carboxyphenyl)methylene)-2-thioxo-4-thiazolidinone
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C482900
name:
  Drug.CTD_v4_cfa_gskb_MESH:C482900_3-((3-trifluoromethyl)phenyl)-5-((3-carboxyphenyl)methylene)-2-thioxo-4-thiazolidinone


id: 75
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C541506
name:
  Drug.CTD_v4_cfa_gskb_MESH:C541506_3-(6-isobutyl-9-methoxy-1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino(1',2'-1,6)pyrido(3,4-b)indol-3-yl)propionic_acid_tert-butyl_ester

description:
  MESH:C541506 3-(6-isobutyl-9-methoxy-1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino(1',2'-1,6)pyrido(3,4-b)indol-3-yl)propionic acid tert-butyl ester


id: 76
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C562242
name:
  Drug.CTD_v4_cfa_gskb_MESH:C562242_3-(7-trifluoromethyl-5-(2-trifluoromethylphenyl)-1H-benzimidazol-2-yl)-1-oxa-2-azaspiro(4.5)dec-2-ene

description:
  MESH:C562242 3-(7-trifluoromethyl-5-(2-trifluoromethylphenyl)-1H-benzimidazol-2-yl)-1-oxa-2-azaspiro(4.5)dec-2-ene


id: 78
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C070417
name:
  Drug.CTD_v4_cfa_gskb_MESH:C070417_(3R)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone

description:
  MESH:C070417 (3R)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone


id: 79
description: MESH:C528564 4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-ylbut-2-enyloxy)acetic acid
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C528564
name:
  Drug.CTD_v4_cfa_gskb_MESH:C528564_4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-ylbut-2-enyloxy)acetic_acid


id: 83
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C483032
name:
  Drug.CTD_v4_cfa_gskb_MESH:C483032_5-(3-methoxyphenyl)-3-(5-methyl-1,2,4-oxadiazol-3-yl)-2-oxo-1,2-dihydro-1,6-naphthyridine

description:
  MESH:C483032 5-(3-methoxyphenyl)-3-(5-methyl-1,2,4-oxadiazol-3-yl)-2-oxo-1,2-dihydro-1,6-naphthyridine


id: 85
n: 2
memo: https://ctdbase.org/detail.go?type=chem&acc=C475093
name:
  Drug.CTD_v4_cfa_gskb_MESH:C475093_6-(4-chlorophenyl)imidazo(2,1-b)(1,3)thiazole-5-carbaldehyde_O-(3,4-dichlorobenzyl)oxime

description:
  MESH:C475093 6-(4-chlorophenyl)imidazo(2,1-b)(1,3)thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime


id: 124
description: MESH:C403753 benzyloxycarbonyl-isoleucyl-glutamyl-threonyl-aspartic acid fluoromethyl ketone
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C403753
name:
  Drug.CTD_v4_cfa_gskb_MESH:C403753_benzyloxycarbonyl-isoleucyl-glutamyl-threonyl-aspartic_acid_fluoromethyl_ketone


id: 125
description: MESH:C403754 benzyloxycarbonyl-leucyl-glutamyl-histidyl-aspartic acid fluoromethyl ketone
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C403754
name:
  Drug.CTD_v4_cfa_gskb_MESH:C403754_benzyloxycarbonyl-leucyl-glutamyl-histidyl-aspartic_acid_fluoromethyl_ketone


id: 287
n: 8
memo: https://ctdbase.org/detail.go?type=chem&acc=C000597426
name:
  Drug.CTD_v4_cfa_gskb_MESH:C000597426_N-(1,2,3,5,6,7-hexahydro-S-indacen-4-ylcarbamoyl)-4-(2-hydroxy-2-propanyl)-2-furansulfonamide

description:
  MESH:C000597426 N-(1,2,3,5,6,7-hexahydro-S-indacen-4-ylcarbamoyl)-4-(2-hydroxy-2-propanyl)-2-furansulfonamide


id: 290
description: MESH:C475772 N-(4-tert-butylphenyl)-4-(3-chloropyridin-2-yl)tetrahydropyrazine-1(2H)-carboxamide
n: 1
memo: https://ctdbase.org/detail.go?type=chem&acc=C475772
name:
  Drug.CTD_v4_cfa_gskb_MESH:C475772_N-(4-tert-butylphenyl)-4-(3-chloropyridin-2-yl)tetrahydropyrazine-1(2H)-carboxamide


id: 462
description: R-CFA-2404192 Signaling by Type 1 Insulin-like Growth Factor 1 Receptor IGF1R
n: 47
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2404192
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2404192_Signaling_by_Type_1_Insulin-like_Growth_Factor_1_Receptor_IGF1R


id: 465
n: 102
memo: https://reactome.org/PathwayBrowser/#/R-CFA-381426
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-381426_Regulation_of_Insulin-like_Growth_Factor_IGF_transport_and_uptake_by_Insulin-like_Growth_Factor_Binding_Proteins_IGFBPs

description:
  R-CFA-381426 Regulation of Insulin-like Growth Factor IGF transport and uptake by Insulin-like Growth Factor Binding Proteins IGFBPs


id: 548
description: R-CFA-140534 Caspase activation via Death Receptors in the presence of ligand
n: 12
memo: https://reactome.org/PathwayBrowser/#/R-CFA-140534
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-140534_Caspase_activation_via_Death_Receptors_in_the_presence_of_ligand


id: 556
description: R-CFA-5357769 Caspase activation via extrinsic apoptotic signalling pathway
n: 15
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5357769
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5357769_Caspase_activation_via_extrinsic_apoptotic_signalling_pathway


id: 562
description: R-CFA-937072 TRAF6-mediated induction of TAK1 complex within TLR4 complex
n: 16
memo: https://reactome.org/PathwayBrowser/#/R-CFA-937072
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-937072_TRAF6-mediated_induction_of_TAK1_complex_within_TLR4_complex


id: 563
description: R-CFA-975138 TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation
n: 84
memo: https://reactome.org/PathwayBrowser/#/R-CFA-975138
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-975138_TRAF6_mediated_induction_of_NFkB_and_MAP_kinases_upon_TLR7/8_or_9_activation


id: 565
description: R-CFA-975163 IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation
n: 15
memo: https://reactome.org/PathwayBrowser/#/R-CFA-975163
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-975163_IRAK2_mediated_activation_of_TAK1_complex_upon_TLR7/8_or_9_stimulation


id: 566
description: R-CFA-9824878 Regulation of TBK1 IKKÎµ IKBKE-mediated activation of IRF3 IRF7
n: 14
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9824878
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9824878_Regulation_of_TBK1_IKKÎµ_IKBKE-mediated_activation_of_IRF3_IRF7


id: 629
description: R-CFA-156827 L13a-mediated translational silencing of Ceruloplasmin expression
n: 109
memo: https://reactome.org/PathwayBrowser/#/R-CFA-156827
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-156827_L13a-mediated_translational_silencing_of_Ceruloplasmin_expression


id: 630
description: R-CFA-1799339 SRP-dependent cotranslational protein targeting to membrane
n: 89
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1799339
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1799339_SRP-dependent_cotranslational_protein_targeting_to_membrane


id: 631
description: R-CFA-6791226 Major pathway of rRNA processing in the nucleolus and cytosol
n: 141
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6791226
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6791226_Major_pathway_of_rRNA_processing_in_the_nucleolus_and_cytosol


id: 641
description: R-CFA-975956 Nonsense Mediated Decay NMD independent of the Exon Junction Complex EJC
n: 91
memo: https://reactome.org/PathwayBrowser/#/R-CFA-975956
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-975956_Nonsense_Mediated_Decay_NMD_independent_of_the_Exon_Junction_Complex_EJC


id: 642
description: R-CFA-975957 Nonsense Mediated Decay NMD enhanced by the Exon Junction Complex EJC
n: 109
memo: https://reactome.org/PathwayBrowser/#/R-CFA-975957
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-975957_Nonsense_Mediated_Decay_NMD_enhanced_by_the_Exon_Junction_Complex_EJC


id: 644
description: R-CFA-163125 Post-translational modificationsynthesis of GPI-anchored proteins
n: 66
memo: https://reactome.org/PathwayBrowser/#/R-CFA-163125
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-163125_Post-translational_modificationsynthesis_of_GPI-anchored_proteins


id: 668
description: R-CFA-5693567 HDR through Homologous Recombination HRR or Single Strand Annealing SSA
n: 75
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5693567
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5693567_HDR_through_Homologous_Recombination_HRR_or_Single_Strand_Annealing_SSA


id: 669
description: R-CFA-5693568 Resolution of D-loop Structures through Holliday Junction Intermediates
n: 30
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5693568
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5693568_Resolution_of_D-loop_Structures_through_Holliday_Junction_Intermediates


id: 675
description: R-CFA-190840 Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane
n: 13
memo: https://reactome.org/PathwayBrowser/#/R-CFA-190840
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-190840_Microtubule-dependent_trafficking_of_connexons_from_Golgi_to_the_plasma_membrane


id: 686
description: R-CFA-2173791 TGF-beta receptor signaling in EMT epithelial to mesenchymal transition
n: 14
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2173791
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2173791_TGF-beta_receptor_signaling_in_EMT_epithelial_to_mesenchymal_transition


id: 695
description: R-CFA-444473 Formyl peptide receptors bind formyl peptides and many other ligands
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-444473
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-444473_Formyl_peptide_receptors_bind_formyl_peptides_and_many_other_ligands


id: 711
description: R-CFA-9856649 Transcriptional and post-translational regulation of MITF-M expression and activity
n: 26
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9856649
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9856649_Transcriptional_and_post-translational_regulation_of_MITF-M_expression_and_activity


id: 740
description: R-CFA-112314 Neurotransmitter receptors and postsynaptic signal transmission
n: 135
memo: https://reactome.org/PathwayBrowser/#/R-CFA-112314
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-112314_Neurotransmitter_receptors_and_postsynaptic_signal_transmission


id: 750
description: R-CFA-425393 Transport of inorganic cations/anions and amino acids/oligopeptides
n: 105
memo: https://reactome.org/PathwayBrowser/#/R-CFA-425393
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-425393_Transport_of_inorganic_cations/anions_and_amino_acids/oligopeptides


id: 765
description: R-CFA-193368 Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
n: 18
memo: https://reactome.org/PathwayBrowser/#/R-CFA-193368
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-193368_Synthesis_of_bile_acids_and_bile_salts_via_7alpha-hydroxycholesterol


id: 766
description: R-CFA-193775 Synthesis of bile acids and bile salts via 24-hydroxycholesterol
n: 8
memo: https://reactome.org/PathwayBrowser/#/R-CFA-193775
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-193775_Synthesis_of_bile_acids_and_bile_salts_via_24-hydroxycholesterol


id: 780
description: R-CFA-111459 Activation of caspases through apoptosome-mediated cleavage
n: 6
memo: https://reactome.org/PathwayBrowser/#/R-CFA-111459
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-111459_Activation_of_caspases_through_apoptosome-mediated_cleavage


id: 784
n: 42
memo: https://reactome.org/PathwayBrowser/#/R-CFA-168643
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-168643_Nucleotide-binding_domain_leucine_rich_repeat_containing_receptor_NLR_signaling_pathways

description:
  R-CFA-168643 Nucleotide-binding domain leucine rich repeat containing receptor NLR signaling pathways


id: 786
description: R-CFA-418889 Caspase activation via Dependence Receptors in the absence of ligand
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-418889
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-418889_Caspase_activation_via_Dependence_Receptors_in_the_absence_of_ligand


id: 804
description: R-CFA-8864260 Transcriptional regulation by the AP-2 TFAP2 family of transcription factors
n: 19
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8864260
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8864260_Transcriptional_regulation_by_the_AP-2_TFAP2_family_of_transcription_factors


id: 805
description: R-CFA-8866910 TFAP2 AP-2 family regulates transcription of growth factors and their receptors
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8866910
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8866910_TFAP2_AP-2_family_regulates_transcription_of_growth_factors_and_their_receptors


id: 814
description: R-CFA-110313 Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template
n: 35
memo: https://reactome.org/PathwayBrowser/#/R-CFA-110313
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-110313_Translesion_synthesis_by_Y_family_DNA_polymerases_bypasses_lesions_on_DNA_template


id: 827
description: R-CFA-983231 Factors involved in megakaryocyte development and platelet production
n: 113
memo: https://reactome.org/PathwayBrowser/#/R-CFA-983231
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-983231_Factors_involved_in_megakaryocyte_development_and_platelet_production


id: 840
description: R-CFA-425366 Transport of bile salts and organic acids metal ions and amine compounds
n: 73
memo: https://reactome.org/PathwayBrowser/#/R-CFA-425366
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-425366_Transport_of_bile_salts_and_organic_acids_metal_ions_and_amine_compounds


id: 873
description: R-CFA-141444 Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
n: 90
memo: https://reactome.org/PathwayBrowser/#/R-CFA-141444
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-141444_Amplification__of_signal_from_unattached__kinetochores_via_a_MAD2__inhibitory_signal


id: 903
description: R-CFA-8939236 RUNX1 regulates transcription of genes involved in differentiation of HSCs
n: 17
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8939236
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8939236_RUNX1_regulates_transcription_of_genes_involved_in_differentiation_of_HSCs


id: 910
description: R-CFA-1234176 Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha
n: 62
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1234176
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1234176_Oxygen-dependent_proline_hydroxylation_of_Hypoxia-inducible_Factor_Alpha


id: 913
description: R-CFA-3371497 HSP90 chaperone cycle for steroid hormone receptors SHR in the presence of ligand
n: 47
memo: https://reactome.org/PathwayBrowser/#/R-CFA-3371497
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-3371497_HSP90_chaperone_cycle_for_steroid_hormone_receptors_SHR_in_the_presence_of_ligand


id: 919
description: R-CFA-8852276 The role of GTSE1 in G2/M progression after G2 checkpoint
n: 64
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8852276
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8852276_The_role_of_GTSE1_in_G2/M_progression_after_G2_checkpoint


id: 920
description: R-CFA-8955332 Carboxyterminal post-translational modifications of tubulin
n: 24
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8955332
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8955332_Carboxyterminal_post-translational_modifications_of_tubulin


id: 939
description: R-CFA-6804116 TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest
n: 9
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6804116
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6804116_TP53_Regulates_Transcription_of_Genes_Involved_in_G1_Cell_Cycle_Arrest


id: 942
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-69200
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-69200_Phosphorylation_of_proteins_involved_in_G1/S_transition_by_active_Cyclin_E:Cdk2_complexes

description:
  R-CFA-69200 Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes


id: 956
description: R-CFA-5676594 TNF receptor superfamily TNFSF members mediating non-canonical NF-kB pathway
n: 17
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5676594
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5676594_TNF_receptor_superfamily_TNFSF_members_mediating_non-canonical_NF-kB_pathway


id: 982
description: R-CFA-432040 Vasopressin regulates renal water homeostasis via Aquaporins
n: 28
memo: https://reactome.org/PathwayBrowser/#/R-CFA-432040
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-432040_Vasopressin_regulates_renal_water_homeostasis_via_Aquaporins


id: 984
description: R-CFA-456926 Thrombin signalling through proteinase activated receptors PARs
n: 26
memo: https://reactome.org/PathwayBrowser/#/R-CFA-456926
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-456926_Thrombin_signalling_through_proteinase_activated_receptors_PARs


id: 986
description: R-CFA-6814122 Cooperation of PDCL PhLP1 and TRiC/CCT in G-protein beta folding
n: 32
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6814122
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6814122_Cooperation_of_PDCL_PhLP1_and_TRiC/CCT_in_G-protein_beta_folding


id: 992
description: R-CFA-997272 Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits
n: 22
memo: https://reactome.org/PathwayBrowser/#/R-CFA-997272
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-997272_Inhibition__of_voltage_gated_Ca2+_channels_via_Gbeta/gamma_subunits


id: 1000
description: R-CFA-9617629 Regulation of FOXO transcriptional activity by acetylation
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9617629
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9617629_Regulation_of_FOXO_transcriptional_activity_by_acetylation


id: 1024
description: R-CFA-198933 Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
n: 89
memo: https://reactome.org/PathwayBrowser/#/R-CFA-198933
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-198933_Immunoregulatory_interactions_between_a_Lymphoid_and_a_non-Lymphoid_cell


id: 1032
description: R-CFA-606279 Deposition of new CENPA-containing nucleosomes at the centromere
n: 26
memo: https://reactome.org/PathwayBrowser/#/R-CFA-606279
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-606279_Deposition_of_new_CENPA-containing_nucleosomes_at_the_centromere


id: 1047
n: 17
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6804115
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6804115_TP53_regulates_transcription_of_additional_cell_cycle_genes_whose_exact_role_in_the_p53_pathway_remain_uncertain

description:
  R-CFA-6804115 TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain


id: 1048
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8869496
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8869496_TFAP2A_acts_as_a_transcriptional_repressor_during_retinoic_acid_induced_cell_differentiation

description:
  R-CFA-8869496 TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation


id: 1052
description: R-CFA-433137 Sodium-coupled sulphate diand tri-carboxylate transporters
n: 5
memo: https://reactome.org/PathwayBrowser/#/R-CFA-433137
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-433137_Sodium-coupled_sulphate_diand_tri-carboxylate_transporters


id: 1082
description: R-CFA-5693616 Presynaptic phase of homologous DNA pairing and strand exchange
n: 21
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5693616
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5693616_Presynaptic_phase_of_homologous_DNA_pairing_and_strand_exchange


id: 1092
description: R-CFA-110381 Resolution of AP sites via the single-nucleotide replacement pathway
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-110381
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-110381_Resolution_of_AP_sites_via_the_single-nucleotide_replacement_pathway


id: 1093
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5649702
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5649702_APEX1-Independent_Resolution_of_AP_Sites_via_the_Single_Nucleotide_Replacement_Pathway

description:
  R-CFA-5649702 APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway


id: 1104
description: R-CFA-73779 RNA Polymerase II Transcription Pre-Initiation And Promoter Opening
n: 43
memo: https://reactome.org/PathwayBrowser/#/R-CFA-73779
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-73779_RNA_Polymerase_II_Transcription_Pre-Initiation_And_Promoter_Opening


id: 1106
description: R-CFA-76042 RNA Polymerase II Transcription Initiation And Promoter Clearance
n: 43
memo: https://reactome.org/PathwayBrowser/#/R-CFA-76042
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-76042_RNA_Polymerase_II_Transcription_Initiation_And_Promoter_Clearance


id: 1108
description: R-CFA-110314 Recognition of DNA damage by PCNA-containing replication complex
n: 29
memo: https://reactome.org/PathwayBrowser/#/R-CFA-110314
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-110314_Recognition_of_DNA_damage_by_PCNA-containing_replication_complex


id: 1109
description: R-CFA-110373 Resolution of AP sites via the multiple-nucleotide patch replacement pathway
n: 22
memo: https://reactome.org/PathwayBrowser/#/R-CFA-110373
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-110373_Resolution_of_AP_sites_via_the_multiple-nucleotide_patch_replacement_pathway


id: 1124
description: R-CFA-8939243 RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
n: 36
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8939243
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8939243_RUNX1_interacts_with_co-factors_whose_precise_effect_on_RUNX1_targets_is_not_known


id: 1128
n: 21
memo: https://reactome.org/PathwayBrowser/#/R-CFA-141405
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-141405_Inhibition_of_the_proteolytic_activity_of_APC/C_required_for_the_onset_of_anaphase_by_mitotic_spindle_checkpoint_components

description:
  R-CFA-141405 Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components


id: 1129
description: R-CFA-141430 Inactivation of APC/C via direct inhibition of the APC/C complex
n: 21
memo: https://reactome.org/PathwayBrowser/#/R-CFA-141430
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-141430_Inactivation_of_APC/C_via_direct_inhibition_of_the_APC/C_complex


id: 1134
n: 69
memo: https://reactome.org/PathwayBrowser/#/R-CFA-174178
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-174178_APC/C:Cdh1_mediated_degradation_of_Cdc20_and_other_APC/C:Cdh1_targeted_proteins_in_late_mitosis/early_G1

description:
  R-CFA-174178 APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1


id: 1136
description: R-CFA-176407 Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase
n: 20
memo: https://reactome.org/PathwayBrowser/#/R-CFA-176407
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-176407_Conversion_from_APC/C:Cdc20_to_APC/C:Cdh1_in_late_anaphase


id: 1137
description: R-CFA-176408 Regulation of APC/C activators between G1/S and early anaphase
n: 35
memo: https://reactome.org/PathwayBrowser/#/R-CFA-176408
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-176408_Regulation_of_APC/C_activators_between_G1/S_and_early_anaphase


id: 1140
description: R-CFA-176814 Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins
n: 73
memo: https://reactome.org/PathwayBrowser/#/R-CFA-176814
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-176814_Activation_of_APC/C_and_APC/C:Cdc20_mediated_degradation_of_mitotic_proteins


id: 1142
n: 70
memo: https://reactome.org/PathwayBrowser/#/R-CFA-179419
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-179419_APC:Cdc20_mediated_degradation_of_cell_cycle_proteins_prior_to_satisfation_of_the_cell_cycle_checkpoint

description:
  R-CFA-179419 APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint


id: 1150
description: R-CFA-2173793 Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer
n: 41
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2173793
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2173793_Transcriptional_activity_of_SMAD2/SMAD3:SMAD4_heterotrimer


id: 1154
description: R-CFA-2022090 Assembly of collagen fibrils and other multimeric structures
n: 35
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2022090
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2022090_Assembly_of_collagen_fibrils_and_other_multimeric_structures


id: 1157
description: R-CFA-2029482 Regulation of actin dynamics for phagocytic cup formation
n: 56
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2029482
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2029482_Regulation_of_actin_dynamics_for_phagocytic_cup_formation


id: 1204
description: R-CFA-381771 Synthesis secretion and inactivation of Glucagon-like Peptide-1 GLP-1
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-381771
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-381771_Synthesis_secretion_and_inactivation_of_Glucagon-like_Peptide-1_GLP-1


id: 1207
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-400511
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-400511_Synthesis_secretion_and_inactivation_of_Glucose-dependent_Insulinotropic_Polypeptide_GIP

description:
  R-CFA-400511 Synthesis secretion and inactivation of Glucose-dependent Insulinotropic Polypeptide GIP


id: 1208
description: R-CFA-434316 Fatty Acids bound to GPR40 FFAR1 regulate insulin secretion
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-434316
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-434316_Fatty_Acids_bound_to_GPR40_FFAR1_regulate_insulin_secretion


id: 1230
description: R-CFA-399721 Glutamate binding activation of AMPA receptors and synaptic plasticity
n: 29
memo: https://reactome.org/PathwayBrowser/#/R-CFA-399721
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-399721_Glutamate_binding_activation_of_AMPA_receptors_and_synaptic_plasticity


id: 1232
description: R-CFA-438066 Unblocking of NMDA receptors glutamate binding and activation
n: 19
memo: https://reactome.org/PathwayBrowser/#/R-CFA-438066
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-438066_Unblocking_of_NMDA_receptors_glutamate_binding_and_activation


id: 1242
n: 58
memo: https://reactome.org/PathwayBrowser/#/R-CFA-72662
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-72662_Activation_of_the_mRNA_upon_binding_of_the_cap-binding_complex_and_eIFs_and_subsequent_binding_to_43S

description:
  R-CFA-72662 Activation of the mRNA upon binding of the cap-binding complex and eIFs and subsequent binding to 43S


id: 1255
n: 69
memo: https://reactome.org/PathwayBrowser/#/R-CFA-446193
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-446193_Biosynthesis_of_the_N-glycan_precursor_dolichol_lipid-linked_oligosaccharide_LLO_and_transfer_to_a_nascent_protein

description:
  R-CFA-446193 Biosynthesis of the N-glycan precursor dolichol lipid-linked oligosaccharide LLO and transfer to a nascent protein


id: 1259
description: R-CFA-975578 Reactions specific to the complex N-glycan synthesis pathway
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-975578
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-975578_Reactions_specific_to_the_complex_N-glycan_synthesis_pathway


id: 1290
description: R-CFA-450321 JNK c-Jun kinases phosphorylation and activation mediated by activated human TAK1
n: 22
memo: https://reactome.org/PathwayBrowser/#/R-CFA-450321
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-450321_JNK_c-Jun_kinases_phosphorylation_and__activation_mediated_by_activated_human_TAK1


id: 1301
description: R-CFA-629587 Highly sodium permeable postsynaptic acetylcholine nicotinic receptors
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-629587
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-629587_Highly_sodium_permeable_postsynaptic_acetylcholine_nicotinic_receptors


id: 1308
description: R-CFA-113501 Inhibition of replication initiation of damaged DNA by RB1/E2F1
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-113501
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-113501_Inhibition_of_replication_initiation_of_damaged_DNA_by_RB1/E2F1


id: 1317
description: R-CFA-4641262 Disassembly of the destruction complex and recruitment of AXIN to the membrane
n: 27
memo: https://reactome.org/PathwayBrowser/#/R-CFA-4641262
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-4641262_Disassembly_of_the_destruction_complex_and_recruitment_of_AXIN_to_the_membrane


id: 1324
description: R-CFA-983695 Antigen activates B Cell Receptor BCR leading to generation of second messengers
n: 23
memo: https://reactome.org/PathwayBrowser/#/R-CFA-983695
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-983695_Antigen_activates_B_Cell_Receptor_BCR_leading_to_generation_of_second_messengers


id: 1332
description: R-CFA-380284 Loss of proteins required for interphase microtubule organization from the centrosome
n: 65
memo: https://reactome.org/PathwayBrowser/#/R-CFA-380284
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-380284_Loss_of_proteins_required_for_interphase_microtubule_organization_from_the_centrosome


id: 1337
description: R-CFA-9634600 Regulation of glycolysis by fructose 26-bisphosphate metabolism
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9634600
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9634600_Regulation_of_glycolysis_by_fructose_26-bisphosphate_metabolism


id: 1346
description: R-CFA-159231 Transport of Mature mRNA Derived from an Intronless Transcript
n: 39
memo: https://reactome.org/PathwayBrowser/#/R-CFA-159231
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-159231_Transport_of_Mature_mRNA_Derived_from_an_Intronless_Transcript


id: 1347
description: R-CFA-159234 Transport of Mature mRNAs Derived from Intronless Transcripts
n: 40
memo: https://reactome.org/PathwayBrowser/#/R-CFA-159234
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-159234_Transport_of_Mature_mRNAs_Derived_from_Intronless_Transcripts


id: 1348
description: R-CFA-159236 Transport of Mature mRNA derived from an Intron-Containing Transcript
n: 39
memo: https://reactome.org/PathwayBrowser/#/R-CFA-159236
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-159236_Transport_of_Mature_mRNA_derived_from_an_Intron-Containing_Transcript


id: 1349
description: R-CFA-170822 Regulation of Glucokinase by Glucokinase Regulatory Protein
n: 29
memo: https://reactome.org/PathwayBrowser/#/R-CFA-170822
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-170822_Regulation_of_Glucokinase_by_Glucokinase_Regulatory_Protein


id: 1367
description: R-CFA-1234158 Regulation of gene expression by Hypoxia-inducible Factor
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1234158
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1234158_Regulation_of_gene_expression_by_Hypoxia-inducible_Factor


id: 1369
description: R-CFA-3134973 LRR FLII-interacting protein 1 LRRFIP1 activates type I IFN production
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-3134973
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-3134973_LRR_FLII-interacting_protein_1_LRRFIP1_activates_type_I_IFN_production


id: 1373
description: R-CFA-8866907 Activation of the TFAP2 AP-2 family of transcription factors
n: 11
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8866907
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8866907_Activation_of_the_TFAP2_AP-2_family_of_transcription_factors


id: 1374
description: R-CFA-8939246 RUNX1 regulates transcription of genes involved in differentiation of myeloid cells
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8939246
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8939246_RUNX1_regulates_transcription_of_genes_involved_in_differentiation_of_myeloid_cells


id: 1389
description: R-CFA-72695 Formation of the ternary complex and subsequently the 43S complex
n: 49
memo: https://reactome.org/PathwayBrowser/#/R-CFA-72695
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-72695_Formation_of_the_ternary_complex_and_subsequently_the_43S_complex


id: 1403
description: R-CFA-1236973 Cross-presentation of particulate exogenous antigens phagosomes
n: 8
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1236973
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1236973_Cross-presentation_of_particulate_exogenous_antigens_phagosomes


id: 1434
description: R-CFA-163841 Gamma carboxylation hypusinylation hydroxylation and arylsulfatase activation
n: 53
memo: https://reactome.org/PathwayBrowser/#/R-CFA-163841
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-163841_Gamma_carboxylation_hypusinylation_hydroxylation_and_arylsulfatase_activation


id: 1443
description: R-CFA-2514859 Inactivation recovery and regulation of the phototransduction cascade
n: 25
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2514859
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2514859_Inactivation_recovery_and_regulation_of_the_phototransduction_cascade


id: 1450
description: R-CFA-6804759 Regulation of TP53 Activity through Association with Co-factors
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6804759
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6804759_Regulation_of_TP53_Activity_through_Association_with_Co-factors


id: 1451
description: R-CFA-8936459 RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
n: 36
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8936459
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8936459_RUNX1_regulates_genes_involved_in_megakaryocyte_differentiation_and_platelet_function


id: 1459
description: R-CFA-9609523 Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
n: 15
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9609523
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9609523_Insertion_of_tail-anchored_proteins_into_the_endoplasmic_reticulum_membrane


id: 1465
description: R-CFA-111453 BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-111453
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-111453_BH3-only_proteins_associate_with_and_inactivate_anti-apoptotic_BCL-2_members


id: 1467
description: R-CFA-983170 Antigen PresentationFolding assembly and peptide loading of class I MHC
n: 21
memo: https://reactome.org/PathwayBrowser/#/R-CFA-983170
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-983170_Antigen_PresentationFolding_assembly_and_peptide_loading_of_class_I_MHC


id: 1487
description: R-CFA-8939242 RUNX1 regulates transcription of genes involved in differentiation of keratinocytes
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8939242
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8939242_RUNX1_regulates_transcription_of_genes_involved_in_differentiation_of_keratinocytes


id: 1489
description: R-CFA-450531 Regulation of mRNA stability by proteins that bind AU-rich elements
n: 77
memo: https://reactome.org/PathwayBrowser/#/R-CFA-450531
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-450531_Regulation_of_mRNA_stability_by_proteins_that_bind_AU-rich_elements


id: 1504
description: R-CFA-532668 N-glycan trimming in the ER and Calnexin/Calreticulin cycle
n: 15
memo: https://reactome.org/PathwayBrowser/#/R-CFA-532668
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-532668_N-glycan_trimming_in_the_ER_and_Calnexin/Calreticulin_cycle


id: 1509
n: 47
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5693565
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5693565_Recruitment_and_ATM-mediated_phosphorylation_of_repair_and_signaling_proteins_at_DNA_double_strand_breaks

description:
  R-CFA-5693565 Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks


id: 1518
description: R-CFA-8854050 FBXL7 down-regulates AURKA during mitotic entry and in early mitosis
n: 51
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8854050
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8854050_FBXL7_down-regulates_AURKA_during_mitotic_entry_and_in_early_mitosis


id: 1537
description: R-CFA-446343 Localization of the PINCH-ILK-PARVIN complex to focal adhesions
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-446343
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-446343_Localization_of_the_PINCH-ILK-PARVIN_complex_to_focal_adhesions


id: 1555
description: R-CFA-77288 mitochondrial fatty acid beta-oxidation of unsaturated fatty acids
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-77288
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-77288_mitochondrial_fatty_acid_beta-oxidation_of_unsaturated_fatty_acids


id: 1566
description: R-CFA-77588 SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs
n: 8
memo: https://reactome.org/PathwayBrowser/#/R-CFA-77588
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-77588_SLBP_Dependent_Processing_of_Replication-Dependent_Histone_Pre-mRNAs


id: 1567
description: R-CFA-1236978 Cross-presentation of soluble exogenous antigens endosomes
n: 44
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1236978
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1236978_Cross-presentation_of_soluble_exogenous_antigens_endosomes


id: 1580
description: R-CFA-450385 Butyrate Response Factor 1 BRF1 binds and destabilizes mRNA
n: 14
memo: https://reactome.org/PathwayBrowser/#/R-CFA-450385
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-450385_Butyrate_Response_Factor_1_BRF1_binds_and_destabilizes_mRNA


id: 1584
description: R-CFA-1971475 A tetrasaccharide linker sequence is required for GAG synthesis
n: 24
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1971475
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1971475_A_tetrasaccharide_linker_sequence_is_required_for_GAG_synthesis


id: 1613
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-83936
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-83936_Transport_of_nucleosides_and_free_purine_and_pyrimidine_bases_across_the_plasma_membrane

description:
  R-CFA-83936 Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane


id: 1633
description: R-CFA-390471 Association of TriC/CCT with target proteins during biosynthesis
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-390471
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-390471_Association_of_TriC/CCT_with_target_proteins_during_biosynthesis


id: 1635
description: R-CFA-1299308 Tandem of pore domain in a weak inwardly rectifying K+ channels TWIK
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1299308
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1299308_Tandem_of_pore_domain_in_a_weak_inwardly_rectifying_K+_channels_TWIK


id: 1644
description: R-CFA-2855086 Ficolins bind to repetitive carbohydrate structures on the target cell surface
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2855086
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2855086_Ficolins_bind_to_repetitive_carbohydrate_structures_on_the_target_cell_surface


id: 1663
description: R-CFA-629594 Highly calcium permeable postsynaptic nicotinic acetylcholine receptors
n: 11
memo: https://reactome.org/PathwayBrowser/#/R-CFA-629594
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-629594_Highly_calcium_permeable_postsynaptic_nicotinic_acetylcholine_receptors


id: 1664
description: R-CFA-629597 Highly calcium permeable nicotinic acetylcholine receptors
n: 9
memo: https://reactome.org/PathwayBrowser/#/R-CFA-629597
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-629597_Highly_calcium_permeable_nicotinic_acetylcholine_receptors


id: 1676
description: R-CFA-442729 CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-442729
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-442729_CREB1_phosphorylation_through_the_activation_of_CaMKII/CaMKK/CaMKIV_cascasde


id: 1685
description: R-CFA-76061 RNA Polymerase III Transcription Initiation From Type 1 Promoter
n: 25
memo: https://reactome.org/PathwayBrowser/#/R-CFA-76061
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-76061_RNA_Polymerase_III_Transcription_Initiation_From_Type_1_Promoter


id: 1686
description: R-CFA-76066 RNA Polymerase III Transcription Initiation From Type 2 Promoter
n: 24
memo: https://reactome.org/PathwayBrowser/#/R-CFA-76066
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-76066_RNA_Polymerase_III_Transcription_Initiation_From_Type_2_Promoter


id: 1687
description: R-CFA-76071 RNA Polymerase III Transcription Initiation From Type 3 Promoter
n: 24
memo: https://reactome.org/PathwayBrowser/#/R-CFA-76071
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-76071_RNA_Polymerase_III_Transcription_Initiation_From_Type_3_Promoter


id: 1689
n: 5
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6803205
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6803205_TP53_regulates_transcription_of_several_additional_cell_death_genes_whose_specific_roles_in_p53-dependent_apoptosis_remain_uncertain

description:
  R-CFA-6803205 TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain


id: 1691
description: R-CFA-75035 Chk1/Chk2Cds1 mediated inactivation of Cyclin B:Cdk1 complex
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-75035
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-75035_Chk1/Chk2Cds1_mediated_inactivation_of_Cyclin_B:Cdk1_complex


id: 1713
description: R-CFA-381340 Transcriptional regulation of white adipocyte differentiation
n: 5
memo: https://reactome.org/PathwayBrowser/#/R-CFA-381340
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-381340_Transcriptional_regulation_of_white_adipocyte_differentiation


id: 1715
description: R-CFA-9029569 NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux
n: 13
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9029569
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9029569_NR1H3_&_NR1H2_regulate_gene_expression_linked_to_cholesterol_transport_and_efflux


id: 1716
description: R-CFA-9623433 NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9623433
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9623433_NR1H2_&_NR1H3_regulate_gene_expression_to_control_bile_acid_homeostasis


id: 1721
description: R-CFA-8866904 Negative regulation of activity of TFAP2 AP-2 family transcription factors
n: 6
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8866904
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8866904_Negative_regulation_of_activity_of_TFAP2_AP-2_family_transcription_factors


id: 1730
description: R-CFA-442742 CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling
n: 5
memo: https://reactome.org/PathwayBrowser/#/R-CFA-442742
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-442742_CREB1_phosphorylation_through_NMDA_receptor-mediated_activation_of_RAS_signaling


id: 1742
description: R-CFA-9824594 Regulation of MITF-M-dependent genes involved in apoptosis
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9824594
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9824594_Regulation_of_MITF-M-dependent_genes_involved_in_apoptosis


id: 1743
description: R-CFA-9825892 Regulation of MITF-M-dependent genes involved in cell cycle and proliferation
n: 8
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9825892
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9825892_Regulation_of_MITF-M-dependent_genes_involved_in_cell_cycle_and_proliferation


id: 1759
description: R-CFA-9026762 Biosynthesis of maresin conjugates in tissue regeneration MCTR
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9026762
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9026762_Biosynthesis_of_maresin_conjugates_in_tissue_regeneration_MCTR


id: 1760
n: 1
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9026766
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9026766_Biosynthesis_of_protectin_and_resolvin_conjugates_in_tissue_regeneration_PCTR_and_RCTR

description:
  R-CFA-9026766 Biosynthesis of protectin and resolvin conjugates in tissue regeneration PCTR and RCTR


id: 1773
description: R-CFA-446388 Regulation of cytoskeletal remodeling and cell spreading by IPP complex components
n: 8
memo: https://reactome.org/PathwayBrowser/#/R-CFA-446388
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-446388_Regulation_of_cytoskeletal_remodeling_and_cell_spreading_by_IPP_complex_components


id: 1780
description: R-CFA-77286 mitochondrial fatty acid beta-oxidation of saturated fatty acids
n: 9
memo: https://reactome.org/PathwayBrowser/#/R-CFA-77286
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-77286_mitochondrial_fatty_acid_beta-oxidation_of_saturated_fatty_acids


id: 1788
description: R-CFA-9764260 Regulation of Expression and Function of Type II Classical Cadherins
n: 12
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9764260
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9764260_Regulation_of_Expression_and_Function_of_Type_II_Classical_Cadherins


id: 1793
description: R-CFA-6803204 TP53 Regulates Transcription of Genes Involved in Cytochrome C Release
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6803204
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6803204_TP53_Regulates_Transcription_of_Genes_Involved_in_Cytochrome_C_Release


id: 1807
description: R-CFA-110330 Recognition and association of DNA glycosylase with site containing an affected purine
n: 22
memo: https://reactome.org/PathwayBrowser/#/R-CFA-110330
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-110330_Recognition_and_association_of_DNA_glycosylase_with_site_containing_an_affected_purine


id: 1815
description: R-CFA-442720 CREB1 phosphorylation through the activation of Adenylate Cyclase
n: 6
memo: https://reactome.org/PathwayBrowser/#/R-CFA-442720
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-442720_CREB1_phosphorylation_through_the_activation_of_Adenylate_Cyclase


id: 1822
description: R-CFA-6803207 TP53 Regulates Transcription of Caspase Activators and Caspases
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6803207
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6803207_TP53_Regulates_Transcription_of_Caspase_Activators_and_Caspases


id: 1832
description: R-CFA-159782 Removal of aminoterminal propeptides from gamma-carboxylated proteins
n: 9
memo: https://reactome.org/PathwayBrowser/#/R-CFA-159782
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-159782_Removal_of_aminoterminal_propeptides_from_gamma-carboxylated_proteins


id: 1833
description: R-CFA-159854 Gamma-carboxylation transport and amino-terminal cleavage of proteins
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-159854
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-159854_Gamma-carboxylation_transport_and_amino-terminal_cleavage_of_proteins


id: 1848
description: R-CFA-193807 Synthesis of bile acids and bile salts via 27-hydroxycholesterol
n: 10
memo: https://reactome.org/PathwayBrowser/#/R-CFA-193807
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-193807_Synthesis_of_bile_acids_and_bile_salts_via_27-hydroxycholesterol


id: 1849
description: R-CFA-9634638 Estrogen-dependent nuclear events downstream of ESR-membrane signaling
n: 5
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9634638
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9634638_Estrogen-dependent_nuclear_events_downstream_of_ESR-membrane_signaling


id: 1851
n: 22
memo: https://reactome.org/PathwayBrowser/#/R-CFA-5625886
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-5625886_Activated_PKN1_stimulates_transcription_of_AR_androgen_receptor_regulated_genes_KLK2_and_KLK3

description:
  R-CFA-5625886 Activated PKN1 stimulates transcription of AR androgen receptor regulated genes KLK2 and KLK3


id: 1853
description: R-CFA-9843970 Regulation of endogenous retroelements by the Human Silencing Hub HUSH complex
n: 22
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9843970
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9843970_Regulation_of_endogenous_retroelements_by_the_Human_Silencing_Hub_HUSH_complex


id: 1855
description: R-CFA-399955 SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion
n: 9
memo: https://reactome.org/PathwayBrowser/#/R-CFA-399955
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-399955_SEMA3A-Plexin_repulsion_signaling_by_inhibiting_Integrin_adhesion


id: 1861
description: R-CFA-2046104 alpha-linolenic omega3 and linoleic omega6 acid metabolism
n: 13
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2046104
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2046104_alpha-linolenic_omega3_and_linoleic_omega6_acid_metabolism


id: 1887
n: 8
memo: https://reactome.org/PathwayBrowser/#/R-CFA-159763
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-159763_Transport_of_gamma-carboxylated_protein_precursors_from_the_endoplasmic_reticulum_to_the_Golgi_apparatus

description:
  R-CFA-159763 Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus


id: 1894
description: R-CFA-8877330 RUNX1 and FOXP3 control the development of regulatory T lymphocytes Tregs
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8877330
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8877330_RUNX1_and_FOXP3_control_the_development_of_regulatory_T_lymphocytes_Tregs


id: 1896
description: R-CFA-8939245 RUNX1 regulates transcription of genes involved in BCR signaling
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8939245
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8939245_RUNX1_regulates_transcription_of_genes_involved_in_BCR_signaling


id: 1897
description: R-CFA-8939247 RUNX1 regulates transcription of genes involved in interleukin signaling
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8939247
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8939247_RUNX1_regulates_transcription_of_genes_involved_in_interleukin_signaling


id: 1902
description: R-CFA-2559584 Formation of Senescence-Associated Heterochromatin Foci SAHF
n: 12
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2559584
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2559584_Formation_of_Senescence-Associated_Heterochromatin_Foci_SAHF


id: 1916
description: R-CFA-73930 Abasic sugar-phosphate removal via the single-nucleotide replacement pathway
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-73930
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-73930_Abasic_sugar-phosphate_removal_via_the_single-nucleotide_replacement_pathway


id: 1918
description: R-CFA-75108 Activation myristolyation of BID and translocation to mitochondria
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-75108
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-75108_Activation_myristolyation_of_BID_and_translocation_to_mitochondria


id: 1925
description: R-CFA-416550 Sema4D mediated inhibition of cell attachment and migration
n: 9
memo: https://reactome.org/PathwayBrowser/#/R-CFA-416550
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-416550_Sema4D_mediated_inhibition_of_cell_attachment_and_migration


id: 1927
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-964827
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-964827_Progressive_trimming_of_alpha-12-linked_mannose_residues_from_Man9/8/7GlcNAc2_to_produce_Man5GlcNAc2

description:
  R-CFA-964827 Progressive trimming of alpha-12-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2


id: 1950
description: R-CFA-9619665 EGR2 and SOX10-mediated initiation of Schwann cell myelination
n: 1
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9619665
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9619665_EGR2_and_SOX10-mediated_initiation_of_Schwann_cell_myelination


id: 1959
description: R-CFA-2142670 Synthesis of epoxy EET and dihydroxyeicosatrienoic acids DHET
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-2142670
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-2142670_Synthesis_of_epoxy_EET_and_dihydroxyeicosatrienoic_acids_DHET


id: 1960
description: R-CFA-9824585 Regulation of MITF-M-dependent genes involved in pigmentation
n: 7
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9824585
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9824585_Regulation_of_MITF-M-dependent_genes_involved_in_pigmentation


id: 1965
description: R-CFA-9717207 Sensory perception of sweet bitter and umami glutamate taste
n: 18
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9717207
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9717207_Sensory_perception_of_sweet_bitter_and_umami_glutamate_taste


id: 1974
description: R-CFA-8866911 TFAP2 AP-2 family regulates transcription of cell cycle factors
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8866911
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8866911_TFAP2_AP-2_family_regulates_transcription_of_cell_cycle_factors


id: 1991
description: R-CFA-6804114 TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-6804114
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-6804114_TP53_Regulates_Transcription_of_Genes_Involved_in_G2_Cell_Cycle_Arrest


id: 2000
description: R-CFA-1474151 Tetrahydrobiopterin BH4 synthesis recycling salvage and regulation
n: 4
memo: https://reactome.org/PathwayBrowser/#/R-CFA-1474151
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-1474151_Tetrahydrobiopterin_BH4_synthesis_recycling_salvage_and_regulation


id: 2007
description: R-CFA-432030 Transport of glycerol from adipocytes to the liver by Aquaporins
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-432030
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-432030_Transport_of_glycerol_from_adipocytes_to_the_liver_by_Aquaporins


id: 2024
description: R-CFA-9615017 FOXO-mediated transcription of oxidative stress metabolic and neuronal genes
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-9615017
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-9615017_FOXO-mediated_transcription_of_oxidative_stress_metabolic_and_neuronal_genes


id: 2037
description: R-CFA-163754 Insulin effects increased synthesis of Xylulose-5-Phosphate
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-163754
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-163754_Insulin_effects_increased_synthesis_of_Xylulose-5-Phosphate


id: 2042
description: R-CFA-3134963 DEx/H-box helicases activate type I IFN and inflammatory cytokines production
n: 6
memo: https://reactome.org/PathwayBrowser/#/R-CFA-3134963
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-3134963_DEx/H-box_helicases_activate_type_I_IFN_and_inflammatory_cytokines_production


id: 2049
description: R-CFA-434313 Intracellular metabolism of fatty acids regulates insulin secretion
n: 3
memo: https://reactome.org/PathwayBrowser/#/R-CFA-434313
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-434313_Intracellular_metabolism_of_fatty_acids_regulates_insulin_secretion


id: 2051
description: R-CFA-8941413 Events associated with phagocytolytic activity of PMN cells
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-8941413
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-8941413_Events_associated_with_phagocytolytic_activity_of_PMN_cells


id: 2066
description: R-CFA-389397 Orexin and neuropeptides FF and QRFP bind to their respective receptors
n: 5
memo: https://reactome.org/PathwayBrowser/#/R-CFA-389397
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-389397_Orexin_and_neuropeptides_FF_and_QRFP_bind_to_their_respective_receptors


id: 2110
description: R-CFA-141333 Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB
n: 2
memo: https://reactome.org/PathwayBrowser/#/R-CFA-141333
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-141333_Biogenic_amines_are_oxidatively_deaminated_to_aldehydes_by_MAOA_and_MAOB


id: 2127
n: 1
memo: https://reactome.org/PathwayBrowser/#/R-CFA-110328
name:
  Curated.Reactome_v4_cfa_gskb_R-CFA-110328_Recognition_and_association_of_DNA_glycosylase_with_site_containing_an_affected_pyrimidine

description:
  R-CFA-110328 Recognition and association of DNA glycosylase with site containing an affected pyrimidine


id: 2178
description: DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2
n: 40
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070434
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070434_hyperphosphatasia_with_impaired_intellectual_development_syndrome_2


id: 2202
description: DOID:9002795 Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy
n: 62
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002795
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002795_Progressive_Microcephaly_with_Seizures_and_Cerebral_and_Cerebellar_Atrophy


id: 2372
description: DOID:9009086 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1
n: 44
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009086
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009086_Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus_Syndrome_1


id: 2398
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070479
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070479_neurodevelopmental_disorder_with_short_stature_prominent_forehead_and_feeding_difficulties

description:
  DOID:0070479 neurodevelopmental disorder with short stature prominent forehead and feeding difficulties


id: 2447
description: DOID:9000443 Intellectual Developmental Disorder with Autism and Macrocephaly
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000443
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000443_Intellectual_Developmental_Disorder_with_Autism_and_Macrocephaly


id: 2460
description: DOID:9002298 Hypertension Early-Onset Autosomal Dominant with Severe Exacerbation in Pregnancy
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002298
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002298_Hypertension_Early-Onset_Autosomal_Dominant_with_Severe_Exacerbation_in_Pregnancy


id: 2471
description: DOID:9004709 NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES IMPAIRED SPEECH AND HYPOTONIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004709
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004709_NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_IMPAIRED_SPEECH_AND_HYPOTONIA


id: 2608
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001712
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001712_Neurodevelopmental_Disorder_with_or_without_Autistic_Features_and/or_Structural_Brain_Abnormalities

description:
  DOID:9001712 Neurodevelopmental Disorder with or without Autistic Features and/or Structural Brain Abnormalities


id: 2609
description: DOID:0060065 autosomal recessive pyridoxine-refractory sideroblastic anemia 2
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060065
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060065_autosomal_recessive_pyridoxine-refractory_sideroblastic_anemia_2


id: 2610
description: DOID:0080343 autosomal recessive pyridoxine-refractory sideroblastic anemia 3
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080343
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080343_autosomal_recessive_pyridoxine-refractory_sideroblastic_anemia_3


id: 2703
description: DOID:9005075 Spastic Paraplegia and Psychomotor Retardation with or without Seizures
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005075
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005075_Spastic_Paraplegia_and_Psychomotor_Retardation_with_or_without_Seizures


id: 2726
description: DOID:9002730 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY HYPOTONIA AND ABSENT LANGUAGE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002730
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002730_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_HYPOTONIA_AND_ABSENT_LANGUAGE


id: 2792
description: DOID:0111039 hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
n: 18
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111039
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111039_hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase


id: 2876
n: 49
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000240
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000240_T-Cell_Immunodeficiency_Recurrent_Infections_and_Autoimmunity_with_or_without_Cardiac_Malformations

description:
  DOID:9000240 T-Cell Immunodeficiency Recurrent Infections and Autoimmunity with or without Cardiac Malformations


id: 2968
description: DOID:9003108 CEREBELLAR ATAXIA INFANTILE WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003108
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003108_CEREBELLAR_ATAXIA_INFANTILE_WITH_PROGRESSIVE_EXTERNAL_OPHTHALMOPLEGIA


id: 3042
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001147
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001147_Cerebral_Autosomal_Recessive_Arteriopathy_with_Subcortical_Infarcts_and_Leukoencephalopathy

description:
  DOID:9001147 Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy


id: 3070
description: DOID:9009083 NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009083
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009083_NEURODEVELOPMENTAL_DISORDER_WITH_CEREBELLAR_HYPOPLASIA_AND_SPASTICITY


id: 3071
description: DOID:9005393 Alzheimer's Disease Early-Onset with Cerebral Amyloid Angiopathy
n: 5
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005393
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005393_Alzheimer's_Disease_Early-Onset_with_Cerebral_Amyloid_Angiopathy


id: 3075
description: DOID:0112321 alacrima achalasia and impaired intellectual development syndrome
n: 45
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112321
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112321_alacrima_achalasia_and_impaired_intellectual_development_syndrome


id: 3096
description: DOID:9009238 INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009238
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009238_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_HYPERTELORISM_AND_DISTINCTIVE_FACIES


id: 3110
description: DOID:9006455 Generalized Epidermolysis Bullosa Simplex 6 with Scarring and Hair Loss
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006455
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006455_Generalized_Epidermolysis_Bullosa_Simplex_6_with_Scarring_and_Hair_Loss


id: 3221
description: DOID:9009220 NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009220
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009220_NEURODEVELOPMENTAL_DISORDER_WITH_CEREBELLAR_ATROPHY_AND_WITH_OR_WITHOUT_SEIZURES


id: 3240
description: DOID:9002021 Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia Combined
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002021
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002021_Charcot-Marie-Tooth_Peroneal_Muscular_Atrophy_and_Friedreich_Ataxia_Combined


id: 3285
n: 103
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003840
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003840_Recurrent_Infections_with_Encephalopathy_Hepatic_Dysfunction_and_Cardiovascular_Malformations

description:
  DOID:9003840 Recurrent Infections with Encephalopathy Hepatic Dysfunction and Cardiovascular Malformations


id: 3402
description: DOID:0112056 X-linked intellectual disability-short stature-overweight syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112056
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112056_X-linked_intellectual_disability-short_stature-overweight_syndrome


id: 3417
description: DOID:0070537 spastic tetraplegia thin corpus callosum and progressive microcephaly
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070537
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070537_spastic_tetraplegia_thin_corpus_callosum_and_progressive_microcephaly


id: 3512
description: DOID:9008892 Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008892
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008892_Intellectual_Developmental_Disorder_with_Dysmorphic_Facies_and_Ptosis


id: 3555
description: DOID:9007202 NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007202
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007202_NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_CEREBELLAR_HYPOPLASIA


id: 3561
description: DOID:0090110 immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
n: 51
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090110
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090110_immune_dysregulation-polyendocrinopathy-enteropathy-X-linked_syndrome


id: 3563
description: DOID:0112122 X-linked epilepsy with variable learning disabilities and behavior disorders
n: 50
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112122
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112122_X-linked_epilepsy_with_variable_learning_disabilities_and_behavior_disorders


id: 3603
description: DOID:9004336 neurodevelopmental disorder with hearing loss seizures and brain abnormalities
n: 15
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004336
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004336_neurodevelopmental_disorder_with_hearing_loss_seizures_and_brain_abnormalities


id: 3608
description: DOID:9009169 LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009169
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009169_LEUKODYSTROPHY_AND_ACQUIRED_MICROCEPHALY_WITH_OR_WITHOUT_DYSTONIA


id: 3696
description: DOID:0081322 contractures pterygia and spondylocarpotarsal fusion syndrome 1B
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081322
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081322_contractures_pterygia_and_spondylocarpotarsal_fusion_syndrome_1B


id: 3726
description: DOID:9004745 RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES
n: 13
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004745
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004745_RETINAL_DYSTROPHY_WITH_INNER_RETINAL_DYSFUNCTION_AND_GANGLION_CELL_ABNORMALITIES


id: 3739
description: DOID:9001367 NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001367
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001367_NEURODEVELOPMENTAL_DISORDER_WITH_ABSENT_LANGUAGE_AND_VARIABLE_SEIZURES


id: 3839
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005494
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005494_X-linked_Epilepsy_2_with_or_without_Impaired_Intellectual_Development_and_Dysmorphic_Features

description:
  DOID:9005494 X-linked Epilepsy 2 with or without Impaired Intellectual Development and Dysmorphic Features


id: 3851
description: DOID:9002403 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002403
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002403_Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus_Syndrome


id: 3852
description: DOID:9003041 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003041
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003041_Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus_Syndrome_3


id: 3942
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111517
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111517_autosomal_dominant_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_2

description:
  DOID:0111517 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2


id: 3966
description: DOID:0060672 GRN-related frontotemporal lobar degeneration with TDP43 inclusions
n: 12
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060672
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060672_GRN-related_frontotemporal_lobar_degeneration_with_TDP43_inclusions


id: 3974
n: 8
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009063
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009063_Evans_Syndrome_Immunodeficiency_and_Premature_Immunosenescence_associated_with_Tripeptidyl-Peptidase_II_Deficiency

description:
  DOID:9009063 Evans Syndrome Immunodeficiency and Premature Immunosenescence associated with Tripeptidyl-Peptidase II Deficiency


id: 3988
description: DOID:9001434 Focal Segmental Glomerulosclerosis and Neurodevelopmental Syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001434
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001434_Focal_Segmental_Glomerulosclerosis_and_Neurodevelopmental_Syndrome


id: 4044
description: DOID:9001283 RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001283
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001283_RETINAL_DYSTROPHY_AND_IRIS_COLOBOMA_WITH_OR_WITHOUT_CONGENITAL_CATARACT


id: 4063
description: DOID:9000725 Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000725
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000725_Radiohumeral_Fusions_with_Other_Skeletal_and_Craniofacial_Anomalies


id: 4064
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000505
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000505_Intellectual_Developmental_Disorder_with_Dysmorphic_Facies_Seizures_and_Distal_Limb_Anomalies

description:
  DOID:9000505 Intellectual Developmental Disorder with Dysmorphic Facies Seizures and Distal Limb Anomalies


id: 4097
description: DOID:9001596 Arthrogryposis Cleft Palate Craniosynostosis and Impaired Intellectual Development
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001596
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001596_Arthrogryposis_Cleft_Palate_Craniosynostosis_and_Impaired_Intellectual_Development


id: 4107
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008019
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008019_CRANIAL_DYSINNERVATION_DISORDER_CONGENITAL_WITH_ABSENT_CORNEAL_REFLEX_AND_DEVELOPMENTAL_DELAY

description:
  DOID:9008019 CRANIAL DYSINNERVATION DISORDER CONGENITAL WITH ABSENT CORNEAL REFLEX AND DEVELOPMENTAL DELAY


id: 4196
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081430
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081430_intellectual_developmental_disorder_with_autistic_features_and_language_delay_with_or_without_seizures

description:
  DOID:0081430 intellectual developmental disorder with autistic features and language delay with or without seizures


id: 4220
description: DOID:9000699 Familial Hypercholesterolemia due to Ligand-Defective Apolipoprotein B
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000699
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000699_Familial_Hypercholesterolemia_due_to_Ligand-Defective_Apolipoprotein_B


id: 4246
description: DOID:0090008 immunodeficiency-centromeric instability-facial anomalies syndrome 1
n: 8
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090008
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090008_immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1


id: 4299
description: DOID:9003448 NEURODEVELOPMENTAL DISORDER WITH SPASTICITY CATARACTS AND CEREBELLAR HYPOPLASIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003448
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003448_NEURODEVELOPMENTAL_DISORDER_WITH_SPASTICITY_CATARACTS_AND_CEREBELLAR_HYPOPLASIA


id: 4398
description: DOID:0111864 autosomal recessive congenital bilateral absence of vas deferens
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111864
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111864_autosomal_recessive_congenital_bilateral_absence_of_vas_deferens


id: 4401
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090014
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090014_severe_combined_immunodeficiency_autosomal_recessive_T_cell-negative_B_cell-positive_NK_cell-positive

description:
  DOID:0090014 severe combined immunodeficiency autosomal recessive T cell-negative B cell-positive NK cell-positive


id: 4411
description: DOID:9007856 Short Stature Auditory Canal Atresia Mandibular Hypoplasia Skeletal Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007856
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007856_Short_Stature_Auditory_Canal_Atresia_Mandibular_Hypoplasia_Skeletal_Abnormalities


id: 4490
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008807
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008807_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_BRAIN_ANOMALIES_DISTINCTIVE_FACIES_AND_ABSENT_LANGUAGE

description:
  DOID:9008807 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA BRAIN ANOMALIES DISTINCTIVE FACIES AND ABSENT LANGUAGE


id: 4523
description: DOID:9002789 INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC SNIJDERS BLOK TYPE
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002789
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002789_INTELLECTUAL_DEVELOPMENTAL_DISORDER_X-LINKED_SYNDROMIC_SNIJDERS_BLOK_TYPE


id: 4557
description: DOID:9005951 NEURODEVELOPMENTAL DISORDER WITH SPASTICITY SEIZURES AND BRAIN ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005951
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005951_NEURODEVELOPMENTAL_DISORDER_WITH_SPASTICITY_SEIZURES_AND_BRAIN_ABNORMALITIES


id: 4558
description: DOID:9008781 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY MOVEMENT ABNORMALITIES AND SEIZURES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008781
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008781_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_MOVEMENT_ABNORMALITIES_AND_SEIZURES


id: 4589
description: DOID:9005237 Autoinflammation Antibody Deficiency and Immune Dysregulation PLCG2-Associated
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005237
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005237_Autoinflammation_Antibody_Deficiency_and_Immune_Dysregulation_PLCG2-Associated


id: 4644
description: DOID:0081175 short stature hearing loss retinitis pigmentosa and distinctive facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081175
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081175_short_stature_hearing_loss_retinitis_pigmentosa_and_distinctive_facies


id: 4651
description: DOID:9009196 Cerebellar Atrophy with Seizures and Variable Developmental Delay
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009196
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009196_Cerebellar_Atrophy_with_Seizures_and_Variable_Developmental_Delay


id: 4656
description: DOID:9009099 NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009099
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009099_NEURODEVELOPMENTAL_DISORDER_WITH_SEVERE_MOTOR_IMPAIRMENT_AND_ABSENT_LANGUAGE


id: 4756
n: 22
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001150
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001150_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_ARTHROGRYPOSIS_AND_STRUCTURAL_BRAIN_ANOMALIES

description:
  DOID:9001150 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY ARTHROGRYPOSIS AND STRUCTURAL BRAIN ANOMALIES


id: 4792
description: DOID:9001227 Pulmonary Arterial Hypertension Hereditary Hemorrhagic Telangiectasia-Related
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001227
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001227_Pulmonary_Arterial_Hypertension_Hereditary_Hemorrhagic_Telangiectasia-Related


id: 4857
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112013
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112013_autosomal_dominant_mutilating_palmoplantar_keratoderma_with_periorificial_keratotic_plaques

description:
  DOID:0112013 autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques


id: 4871
n: 9
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090013
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090013_severe_combined_immunodeficiency_autosomal_recessive_T_cell-negative_B_cell-negative_NK_cell-positive

description:
  DOID:0090013 severe combined immunodeficiency autosomal recessive T cell-negative B cell-negative NK cell-positive


id: 4872
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003214
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003214_Severe_Combined_Immunodeficiency_Autosomal_Recessive_T_Cell-Negative_B_Cell-Positive_NK_Cell-Negative

description:
  DOID:9003214 Severe Combined Immunodeficiency Autosomal Recessive T Cell-Negative B Cell-Positive NK Cell-Negative


id: 4948
description: DOID:9009221 NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009221
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009221_NEURODEVELOPMENTAL_DISORDER_WITH_EPILEPSY_AND_HYPOPLASIA_OF_THE_CORPUS_CALLOSUM


id: 4985
description: DOID:9000988 Infantile-Onset Multisystem Neurologic Endocrine and Pancreatic Disease 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000988
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000988_Infantile-Onset_Multisystem_Neurologic_Endocrine_and_Pancreatic_Disease_2


id: 4987
description: DOID:9006461 Infantile-Onset Multisystem Neurologic Endocrine and Pancreatic Disease
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006461
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006461_Infantile-Onset_Multisystem_Neurologic_Endocrine_and_Pancreatic_Disease


id: 4997
description: DOID:9007151 Chronic recurrent multifocal osteomyelitis 2 with periostitis and pustulosis
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007151
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007151_Chronic_recurrent_multifocal_osteomyelitis_2_with_periostitis_and_pustulosis


id: 5025
description: DOID:9005641 GLOBAL DEVELOPMENTAL DELAY ABSENT OR HYPOPLASTIC CORPUS CALLOSUM AND DYSMORPHIC FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005641
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005641_GLOBAL_DEVELOPMENTAL_DELAY_ABSENT_OR_HYPOPLASTIC_CORPUS_CALLOSUM_AND_DYSMORPHIC_FACIES


id: 5056
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002035
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002035_Stomatin-Deficient_Cryohydrocytosis_with_Mental_Retardation_Seizures_Cataracts_and_Massive_Hepatosplenomegaly

description:
  DOID:9002035 Stomatin-Deficient Cryohydrocytosis with Mental Retardation Seizures Cataracts and Massive Hepatosplenomegaly


id: 5074
description: DOID:0111582 hereditary arterial and articular multiple calcification syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111582
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111582_hereditary_arterial_and_articular_multiple_calcification_syndrome


id: 5088
description: DOID:9003965 NEURODEVELOPMENTAL DISORDER WITH INTRACRANIAL HEMORRHAGE SEIZURES AND SPASTICITY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003965
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003965_NEURODEVELOPMENTAL_DISORDER_WITH_INTRACRANIAL_HEMORRHAGE_SEIZURES_AND_SPASTICITY


id: 5107
description: DOID:9004820 Uridine 5-Prime Monophosphate Hydrolase Deficiency Hemolytic Anemia due to
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004820
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004820_Uridine_5-Prime_Monophosphate_Hydrolase_Deficiency_Hemolytic_Anemia_due_to


id: 5164
description: DOID:9004868 Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities
n: 19
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004868
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004868_Developmental_Delay_with_Variable_Intellectual_Impairment_and_Behavioral_Abnormalities


id: 5190
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111524
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111524_autosomal_recessive_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_5

description:
  DOID:0111524 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5


id: 5191
description: DOID:9009217 Microcephaly Growth Restriction and Increased Sister Chromatid Exchange 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009217
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009217_Microcephaly_Growth_Restriction_and_Increased_Sister_Chromatid_Exchange_2


id: 5200
description: DOID:0070538 syndromic X-linked intellectual developmental disorder Bain type
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070538
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070538_syndromic_X-linked_intellectual_developmental_disorder_Bain_type


id: 5202
description: DOID:9008407 ROLANDIC EPILEPSY INTELLECTUAL DISABILITY AND SPEECH DYSPRAXIA X-LINKED
n: 15
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008407
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008407_ROLANDIC_EPILEPSY_INTELLECTUAL_DISABILITY_AND_SPEECH_DYSPRAXIA_X-LINKED


id: 5254
description: DOID:9000579 INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT PERIPHERAL NEUROPATHY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000579
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000579_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_OR_WITHOUT_PERIPHERAL_NEUROPATHY


id: 5266
description: DOID:0111815 low molecular weight proteinuria with hypercalciuric nephrocalcinosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111815
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111815_low_molecular_weight_proteinuria_with_hypercalciuric_nephrocalcinosis


id: 5328
description: DOID:9000211 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA SEIZURES AND ABSENT LANGUAGE
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000211
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000211_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_SEIZURES_AND_ABSENT_LANGUAGE


id: 5338
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111520
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111520_autosomal_dominant_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_3

description:
  DOID:0111520 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3


id: 5340
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005815
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005815_Progressive_External_Ophthalmoplegia_with_Mitochondrial_DNA_Deletions_Autosomal_Recessive

description:
  DOID:9005815 Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions Autosomal Recessive


id: 5371
description: DOID:0050881 inclusion body myopathy with Paget disease of bone and frontotemporal dementia
n: 5
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0050881
name:
  Disease.RGD_v4_cfa_gskb_DOID:0050881_inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia


id: 5372
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111384
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111384_inclusion_body_myopathy_with_early-onset_Paget_disease_of_bone_with_or_without_frontotemporal_dementia_2

description:
  DOID:0111384 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2


id: 5375
description: DOID:9003549 Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type)
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003549
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003549_Thiamine_Metabolism_Dysfunction_Syndrome_5_(Episodic_Encephalopathy_Type)


id: 5418
description: DOID:9004881 Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004881
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004881_Intellectual_Developmental_Disorder_with_Speech_Delay_and_Axonal_Peripheral_Neuropathy


id: 5466
description: DOID:9006967 Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006967
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006967_Generalized_Hypertrichosis_Terminalis_with_or_without_Gingival_Hyperplasia


id: 5473
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009096
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009096_Neurodevelopmental_Disorder_with_Ataxic_Gait_Absent_Speech_and_Decreased_Cortical_White_Matter

description:
  DOID:9009096 Neurodevelopmental Disorder with Ataxic Gait Absent Speech and Decreased Cortical White Matter


id: 5478
description: DOID:9005912 Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005912
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005912_Nonspherocytic_Hemolytic_Anemia_due_to_Glucose_Phosphate_Isomerase_Deficiency


id: 5514
description: DOID:0070431 hyperphosphatasia with impaired intellectual development syndrome
n: 6
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070431
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070431_hyperphosphatasia_with_impaired_intellectual_development_syndrome


id: 5515
description: DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1
n: 5
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070433
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070433_hyperphosphatasia_with_impaired_intellectual_development_syndrome_1


id: 5517
description: DOID:9001288 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001288
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001288_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_DYSMORPHIC_FACIES


id: 5646
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004662
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004662_Autosomal_Recessive_Syndrome_of_Syndactyly_Undescended_Testes_and_Central_Nervous_System_Defects

description:
  DOID:9004662 Autosomal Recessive Syndrome of Syndactyly Undescended Testes and Central Nervous System Defects


id: 5682
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001503
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001503_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_NEONATAL_RESPIRATORY_INSUFFICIENCY_AND_THERMODYSREGULATION

description:
  DOID:9001503 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA NEONATAL RESPIRATORY INSUFFICIENCY AND THERMODYSREGULATION


id: 5716
description: DOID:0081072 craniofacial dysmorphism skeletal anomalies and mental retardation syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081072
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081072_craniofacial_dysmorphism_skeletal_anomalies_and_mental_retardation_syndrome


id: 5717
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081124
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081124_craniofacial_dysmorphism_skeletal_anomalies_and_impaired_intellectual_development_syndrome_1

description:
  DOID:0081124 craniofacial dysmorphism skeletal anomalies and impaired intellectual development syndrome 1


id: 5742
description: DOID:9009062 Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009062
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009062_Progressive_Early-Onset_Encephalopathy_with_Episodic_Rhabdomyolysis


id: 5759
description: DOID:9006994 INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006994
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006994_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_PERSISTENCE_OF_FETAL_HEMOGLOBIN


id: 5793
description: DOID:0081277 diffuse pediatric-type high-grade glioma H3-wildtype and IDH-wildtype
n: 12
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081277
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081277_diffuse_pediatric-type_high-grade_glioma_H3-wildtype_and_IDH-wildtype


id: 5803
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003704
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003704_Intellectual_Developmental_Disorder_with_Nasal_Speech_Dysmorphic_Facies_and_Variable_Skeletal_Anomalies

description:
  DOID:9003704 Intellectual Developmental Disorder with Nasal Speech Dysmorphic Facies and Variable Skeletal Anomalies


id: 5824
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001649
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001649_Infantile_Cataract_Skin_Abnormalities_Glutamate_Excess_and_Impaired_Intellectual_Development

description:
  DOID:9001649 Infantile Cataract Skin Abnormalities Glutamate Excess and Impaired Intellectual Development


id: 5825
description: DOID:9005979 Global Developmental Delay Progressive Ataxia and Elevated Glutamine
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005979
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005979_Global_Developmental_Delay_Progressive_Ataxia_and_Elevated_Glutamine


id: 5838
description: DOID:9000100 NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000100
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000100_NEURODEVELOPMENTAL_DISORDER_WITH_HYPERKINETIC_MOVEMENTS_AND_DYSKINESIA


id: 5852
description: DOID:0110001 3-methylglutaconic aciduria with deafness encephalopathy and Leigh-like syndrome
n: 26
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0110001
name:
  Disease.RGD_v4_cfa_gskb_DOID:0110001_3-methylglutaconic_aciduria_with_deafness_encephalopathy_and_Leigh-like_syndrome


id: 5871
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004839
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004839_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_GASTROINTESTINAL_DIFFICULTIES_AND_HIGH_PAIN_THRESHOLD

description:
  DOID:9004839 INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD


id: 5874
description: DOID:0080664 diaphyseal medullary stenosis with malignant fibrous histiocytoma
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080664
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080664_diaphyseal_medullary_stenosis_with_malignant_fibrous_histiocytoma


id: 5889
description: DOID:9005015 NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005015
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005015_NEURODEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AND_BEHAVIORAL_ABNORMALITIES


id: 5919
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006438
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006438_Microspherophakia_and/or_Megalocornea_with_Ectopia_Lentis_and_with_or_without_Secondary_Glaucoma

description:
  DOID:9006438 Microspherophakia and/or Megalocornea with Ectopia Lentis and with or without Secondary Glaucoma


id: 5928
description: DOID:9002186 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2
n: 16
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002186
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002186_Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus_Syndrome_2


id: 5950
description: DOID:0070346 neurodevelopmental disorder with cataracts poor growth and dysmorphic facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070346
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070346_neurodevelopmental_disorder_with_cataracts_poor_growth_and_dysmorphic_facies


id: 5982
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000637
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000637_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_VARIABLE_INTELLECTUAL_AND_BEHAVIORAL_ABNORMALITIES

description:
  DOID:9000637 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES


id: 5986
description: DOID:9006620 Leukoencephalopathy Motor Delay Spasticity and Dysarthria Syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006620
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006620_Leukoencephalopathy_Motor_Delay_Spasticity_and_Dysarthria_Syndrome


id: 6011
description: DOID:9005194 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY HYPOTONIA AND VARIABLE BRAIN ANOMALIES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005194
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005194_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_HYPOTONIA_AND_VARIABLE_BRAIN_ANOMALIES


id: 6039
description: DOID:9007416 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY HYPOTONIA NYSTAGMUS AND SEIZURES
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007416
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007416_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_HYPOTONIA_NYSTAGMUS_AND_SEIZURES


id: 6051
description: DOID:9003733 Congenital Adrenal Hyperplasia due to 21 Hydroxylase Deficiency
n: 7
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003733
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003733_Congenital_Adrenal_Hyperplasia_due_to_21_Hydroxylase_Deficiency


id: 6062
description: DOID:9008668 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 3
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008668
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008668_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_3


id: 6089
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001146
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001146_Neurodevelopmental_Disorder_with_Hypotonia_and_Cerebellar_Atrophy_with_or_without_Seizures

description:
  DOID:9001146 Neurodevelopmental Disorder with Hypotonia and Cerebellar Atrophy with or without Seizures


id: 6120
description: DOID:9008787 Intellectual Developmental Disorder with Speech Delay Autism and Dysmorphic Facies
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008787
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008787_Intellectual_Developmental_Disorder_with_Speech_Delay_Autism_and_Dysmorphic_Facies


id: 6133
description: DOID:9005747 Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005747
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005747_Multiple_Congenital_Anomalies/Dysmorphic_Syndrome-Intellectual_Disability


id: 6139
description: DOID:9007607 NEURODEVELOPMENTAL DISORDER WITH CENTRAL HYPOTONIA AND DYSMORPHIC FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007607
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007607_NEURODEVELOPMENTAL_DISORDER_WITH_CENTRAL_HYPOTONIA_AND_DYSMORPHIC_FACIES


id: 6197
description: DOID:9009182 Developmental Delay with or without Dysmorphic Facies and Autism
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009182
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009182_Developmental_Delay_with_or_without_Dysmorphic_Facies_and_Autism


id: 6214
description: DOID:0070514 neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
n: 9
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070514
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070514_neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies


id: 6215
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070536
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070536_neurodevelopmental_disorder_with_hypotonia_language_delay_and_skeletal_defects_with_or_without_seizures

description:
  DOID:0070536 neurodevelopmental disorder with hypotonia language delay and skeletal defects with or without seizures


id: 6235
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000615
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000615_NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_SLEEP_DISTURBANCE_AND_BRAIN_ABNORMALITIES

description:
  DOID:9000615 NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES SLEEP DISTURBANCE AND BRAIN ABNORMALITIES


id: 6256
description: DOID:0111733 pancreatic hypoplasia-diabetes-congenital heart disease syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111733
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111733_pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome


id: 6267
description: DOID:0090011 immunodeficiency-centromeric instability-facial anomalies syndrome 4
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090011
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090011_immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4


id: 6271
description: DOID:0070423 early onset progressive encephalopathy with brain atrophy and thin corpus callosum
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070423
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070423_early_onset_progressive_encephalopathy_with_brain_atrophy_and_thin_corpus_callosum


id: 6311
description: DOID:0060332 mitochondrial complex V (ATP synthase) deficiency nuclear type 3
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060332
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060332_mitochondrial_complex_V_(ATP_synthase)_deficiency_nuclear_type_3


id: 6312
description: DOID:0070463 mitochondrial complex V (ATP synthase) deficiency nuclear type 5
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070463
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070463_mitochondrial_complex_V_(ATP_synthase)_deficiency_nuclear_type_5


id: 6322
description: DOID:9001354 DEVELOPMENTAL DELAY IMPAIRED GROWTH DYSMORPHIC FACIES AND AXONAL NEUROPATHY
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001354
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001354_DEVELOPMENTAL_DELAY_IMPAIRED_GROWTH_DYSMORPHIC_FACIES_AND_AXONAL_NEUROPATHY


id: 6323
description: DOID:9007858 INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC HACKMANN-DI DONATO TYPE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007858
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007858_INTELLECTUAL_DEVELOPMENTAL_DISORDER_X-LINKED_SYNDROMIC_HACKMANN-DI_DONATO_TYPE


id: 6375
description: DOID:9007937 NEURODEVELOPMENTAL DISORDER WITH NEUROMUSCULAR AND SKELETAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007937
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007937_NEURODEVELOPMENTAL_DISORDER_WITH_NEUROMUSCULAR_AND_SKELETAL_ABNORMALITIES


id: 6406
description: DOID:9001957 Keratosis Palmoplantaris with Periodontopathia and Onychogryposis
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001957
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001957_Keratosis_Palmoplantaris_with_Periodontopathia_and_Onychogryposis


id: 6440
description: DOID:9007747 Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007747
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007747_Leukoencephalopathy_with_Brainstem_and_Spinal_Cord_Involvement_and_Lactate_Elevation


id: 6444
description: DOID:0111931 syndactyly-telecanthus-anogenital and renal malformations syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111931
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111931_syndactyly-telecanthus-anogenital_and_renal_malformations_syndrome


id: 6481
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000267
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000267_LANGUAGE_DELAY_AND_ATTENTION_DEFICIT-HYPERACTIVITY_DISORDER/COGNITIVE_IMPAIRMENT_WITH_OR_WITHOUT_CARDIAC_ARRHYTHMIA

description:
  DOID:9000267 LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA


id: 6497
description: DOID:9006177 ARRHYTHMOGENIC CARDIOMYOPATHY WITH VARIABLE ECTODERMAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006177
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006177_ARRHYTHMOGENIC_CARDIOMYOPATHY_WITH_VARIABLE_ECTODERMAL_ABNORMALITIES


id: 6516
description: DOID:9003298 Glutathione Peroxidase Deficiency Hemolytic Anemia possibly due to
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003298
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003298_Glutathione_Peroxidase_Deficiency_Hemolytic_Anemia_possibly_due_to


id: 6532
description: DOID:9001875 Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001875
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001875_Short-Limb_Skeletal_Dysplasia_with_Severe_Combined_Immunodeficiency


id: 6533
description: DOID:9003677 Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003677
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003677_Macrocephaly_with_Multiple_Epiphyseal_Dysplasia_and_Distinctive_Facies


id: 6540
description: DOID:9004585 GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004585
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004585_GLOBAL_DEVELOPMENTAL_DELAY_WITH_SPEECH_AND_BEHAVIORAL_ABNORMALITIES


id: 6562
description: DOID:9000289 DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000289
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000289_DEVELOPMENTAL_DELAY_WITH_DYSMORPHIC_FACIES_AND_DENTAL_ANOMALIES


id: 6586
description: DOID:9009180 MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME X-LINKED
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009180
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009180_MULTIPLE_CONGENITAL_ANOMALIES-NEURODEVELOPMENTAL_SYNDROME_X-LINKED


id: 6591
description: DOID:0070417 neurodevelopmental disorder with speech impairment and dysmorphic facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070417
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070417_neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies


id: 6654
description: DOID:9004553 NEURODEGENERATION CHILDHOOD-ONSET WITH CEREBELLAR ATAXIA AND COGNITIVE DECLINE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004553
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004553_NEURODEGENERATION_CHILDHOOD-ONSET_WITH_CEREBELLAR_ATAXIA_AND_COGNITIVE_DECLINE


id: 6655
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007586
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007586_NEURODEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AUTISM_AND_ATTENTION_DEFICIT-HYPERACTIVITY_DISORDER

description:
  DOID:9007586 NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AUTISM AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER


id: 6723
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001680
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001680_SHORT_STATURE_AND_ADVANCED_BONE_AGE_WITH_OR_WITHOUT_EARLY-ONSET_OSTEOARTHRITIS_AND/OR_OSTEOCHONDRITIS_DISSECANS

description:
  DOID:9001680 SHORT STATURE AND ADVANCED BONE AGE WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS


id: 6784
description: DOID:9001861 INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001861
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001861_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_BEHAVIORAL_ABNORMALITIES


id: 6810
description: DOID:0070347 encephalopathy due to defective mitochondrial and peroxisomal fission 1
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070347
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070347_encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_1


id: 6816
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009213
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009213_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_BEHAVIORAL_ABNORMALITIES

description:
  DOID:9009213 INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES


id: 6843
description: DOID:9005399 DEVELOPMENTAL DELAY WITH VARIABLE NEUROLOGIC AND BRAIN ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005399
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005399_DEVELOPMENTAL_DELAY_WITH_VARIABLE_NEUROLOGIC_AND_BRAIN_ABNORMALITIES


id: 6851
description: DOID:0111513 metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111513
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111513_metaphyseal_dysplasia-maxillary_hypoplasia-brachydactyly_syndrome


id: 6854
description: DOID:0080836 growth hormone insensitivity syndrome with immune dysregulation 1
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080836
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080836_growth_hormone_insensitivity_syndrome_with_immune_dysregulation_1


id: 6874
description: DOID:9003865 Microcephaly Short Stature and Polymicrogyria with or without Seizures
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003865
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003865_Microcephaly_Short_Stature_and_Polymicrogyria_with_or_without_Seizures


id: 6885
description: DOID:9004125 Supraumbilical Midabdominal Raphe and Facial Cavernous Hemangiomas
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004125
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004125_Supraumbilical_Midabdominal_Raphe_and_Facial_Cavernous_Hemangiomas


id: 6886
description: DOID:0080948 agenesis of corpus callosum cardiac ocular and genital syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080948
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080948_agenesis_of_corpus_callosum_cardiac_ocular_and_genital_syndrome


id: 6911
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008927
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008927_Epidermolysis_Bullosa_Simplex_4_Localized_or_Generalized_Intermediate_Autosomal_Recessive

description:
  DOID:9008927 Epidermolysis Bullosa Simplex 4 Localized or Generalized Intermediate Autosomal Recessive


id: 6929
description: DOID:0050909 extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0050909
name:
  Disease.RGD_v4_cfa_gskb_DOID:0050909_extranodal_marginal_zone_lymphoma_of_mucosa-associated_lymphoid_tissue


id: 6949
description: DOID:9003245 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003245
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003245_Pseudoxanthoma_Elasticum-Like_Disorder_with_Multiple_Coagulation_Factor_Deficiency


id: 6977
description: DOID:9009167 NEURODEGENERATION EARLY-ONSET WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009167
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009167_NEURODEGENERATION_EARLY-ONSET_WITH_CHOREOATHETOID_MOVEMENTS_AND_MICROCYTIC_ANEMIA


id: 6998
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008164
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008164_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_MUSCLE_TONE_ABNORMALITIES_AND_DISTAL_SKELETAL_DEFECTS

description:
  DOID:9008164 INTELLECTUAL DEVELOPMENTAL DISORDER WITH MUSCLE TONE ABNORMALITIES AND DISTAL SKELETAL DEFECTS


id: 7008
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081262
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081262_intellectual_developmental_disorder_with_hypotonia_impaired_speech_and_dysmorphic_facies

description:
  DOID:0081262 intellectual developmental disorder with hypotonia impaired speech and dysmorphic facies


id: 7048
description: DOID:9001091 INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001091
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001091_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_IMPAIRED_LANGUAGE_AND_DYSMORPHIC_FACIES


id: 7053
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080319
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080319_X-linked_immunodeficiency_with_magnesium_defect_Epstein-Barr_virus_infection_and_neoplasia

description:
  DOID:0080319 X-linked immunodeficiency with magnesium defect Epstein-Barr virus infection and neoplasia


id: 7069
description: DOID:9001541 Early-Onset Progressive Encephalopathy with Brain Edema and/or Leukoencephalopathy 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001541
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001541_Early-Onset_Progressive_Encephalopathy_with_Brain_Edema_and/or_Leukoencephalopathy_2


id: 7071
description: DOID:0060982 mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060982
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060982_mosaic_variegated_aneuploidy_syndrome_7_with_inflammation_and_tumor_predisposition


id: 7075
description: DOID:9002623 HEMOLYTIC UREMIC SYNDROME ATYPICAL 8 WITH RHIZOMELIC SHORT STATURE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002623
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002623_HEMOLYTIC_UREMIC_SYNDROME_ATYPICAL_8_WITH_RHIZOMELIC_SHORT_STATURE


id: 7080
description: DOID:9008864 POLYMICROGYRIA PERISYLVIAN WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008864
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008864_POLYMICROGYRIA_PERISYLVIAN_WITH_CEREBELLAR_HYPOPLASIA_AND_ARTHROGRYPOSIS


id: 7118
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001294
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001294_NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_SKELETAL_AND_BRAIN_ABNORMALITIES

description:
  DOID:9001294 NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND SKELETAL AND BRAIN ABNORMALITIES


id: 7119
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009077
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009077_NEURODEGENERATION_WITH_DEVELOPMENTAL_DELAY_EARLY_RESPIRATORY_FAILURE_MYOCLONIC_SEIZURES_AND_BRAIN_ABNORMALITIES

description:
  DOID:9009077 NEURODEGENERATION WITH DEVELOPMENTAL DELAY EARLY RESPIRATORY FAILURE MYOCLONIC SEIZURES AND BRAIN ABNORMALITIES


id: 7138
description: DOID:9008326 NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND VARIABLE COGNITIVE ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008326
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008326_NEURODEVELOPMENTAL_DISORDER_WITH_LANGUAGE_DELAY_AND_VARIABLE_COGNITIVE_ABNORMALITIES


id: 7191
description: DOID:0081275 neurodevelopmental disorder with eye movement abnormalities and ataxia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081275
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081275_neurodevelopmental_disorder_with_eye_movement_abnormalities_and_ataxia


id: 7198
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005774
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005774_Alpha/Beta_T-Cell_Lymphopenia_with_Gamma/Delta_T-Cell_Expansion_Severe_Cytomegalovirus_Infection_and_Autoimmunity

description:
  DOID:9005774 Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion Severe Cytomegalovirus Infection and Autoimmunity


id: 7203
description: DOID:9007578 LETM1-ASSOCIATED CLINICAL SPECTRUM WITH PREDOMINANT NERVOUS SYSTEM INVOLVEMENT
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007578
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007578_LETM1-ASSOCIATED_CLINICAL_SPECTRUM_WITH_PREDOMINANT_NERVOUS_SYSTEM_INVOLVEMENT


id: 7204
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007987
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007987_NEURODEGENERATION_CHILDHOOD-ONSET_WITH_MULTISYSTEM_INVOLVEMENT_DUE_TO_MITOCHONDRIAL_DYSFUNCTION

description:
  DOID:9007987 NEURODEGENERATION CHILDHOOD-ONSET WITH MULTISYSTEM INVOLVEMENT DUE TO MITOCHONDRIAL DYSFUNCTION


id: 7255
description: DOID:9000849 Retinal Dystrophy Juvenile Cataracts and Short Stature Syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000849
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000849_Retinal_Dystrophy_Juvenile_Cataracts_and_Short_Stature_Syndrome


id: 7283
description: DOID:0090009 immunodeficiency-centromeric instability-facial anomalies syndrome 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090009
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090009_immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2


id: 7303
description: DOID:9009112 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 5
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009112
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009112_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_5


id: 7309
description: DOID:9006229 MUSCULAR DYSTROPHY CONGENITAL HEARING LOSS AND OVARIAN INSUFFICIENCY SYNDROME
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006229
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006229_MUSCULAR_DYSTROPHY_CONGENITAL_HEARING_LOSS_AND_OVARIAN_INSUFFICIENCY_SYNDROME


id: 7320
description: DOID:9001162 Cutis Verticis Gyrata Retinitis Pigmentosa and Sensorineural Deafness
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001162
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001162_Cutis_Verticis_Gyrata_Retinitis_Pigmentosa_and_Sensorineural_Deafness


id: 7338
description: DOID:0081444 neurodevelopmental disorder with poor growth and behavioral abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081444
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081444_neurodevelopmental_disorder_with_poor_growth_and_behavioral_abnormalities


id: 7343
description: DOID:9007433 INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007433
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007433_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SHORT_STATURE_AND_VARIABLE_SKELETAL_ANOMALIES


id: 7368
description: DOID:9001976 Presynaptic Congenital Myasthenic Syndrome 7B Autosomal Recessive
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001976
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001976_Presynaptic_Congenital_Myasthenic_Syndrome_7B_Autosomal_Recessive


id: 7421
description: DOID:9002826 Somatic Leydig Cell Adenoma with Male-Limited Precocious Puberty
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002826
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002826_Somatic_Leydig_Cell_Adenoma_with_Male-Limited_Precocious_Puberty


id: 7456
description: DOID:9001002 NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001002
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001002_NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_DISTAL_SKELETAL_ANOMALIES


id: 7457
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001418
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001418_INTELLECTUAL_DEVELOPMENTAL_DISORDER_X-LINKED_SYNDROMIC_WITH_PIGMENTARY_MOSAICISM_AND_COARSE_FACIES

description:
  DOID:9001418 INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED SYNDROMIC WITH PIGMENTARY MOSAICISM AND COARSE FACIES


id: 7461
description: DOID:9007455 Congenital Hypotonia Epilepsy Developmental Delay and Digital Anomalies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007455
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007455_Congenital_Hypotonia_Epilepsy_Developmental_Delay_and_Digital_Anomalies


id: 7482
description: DOID:9003092 Glomerulonephritis with Isolated C3 Deposits and Factor H Deficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003092
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003092_Glomerulonephritis_with_Isolated_C3_Deposits_and_Factor_H_Deficiency


id: 7491
description: DOID:9001770 ONYCHODYSTROPHY OSTEODYSTROPHY IMPAIRED INTELLECTUAL DEVELOPMENT AND SEIZURES SYNDROME
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001770
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001770_ONYCHODYSTROPHY_OSTEODYSTROPHY_IMPAIRED_INTELLECTUAL_DEVELOPMENT_AND_SEIZURES_SYNDROME


id: 7498
description: DOID:0081364 neurodegeneration with ataxia dystonia and gaze palsy childhood-onset
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081364
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081364_neurodegeneration_with_ataxia_dystonia_and_gaze_palsy_childhood-onset


id: 7503
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004290
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004290_Neurodevelopmental_Disorder_with_Epilepsy_Cataracts_Feeding_Difficulties_and_Delayed_Brain_Myelination

description:
  DOID:9004290 Neurodevelopmental Disorder with Epilepsy Cataracts Feeding Difficulties and Delayed Brain Myelination


id: 7514
description: DOID:9006716 Neurodevelopmental Disorder with Microcephaly Cortical Malformations and Spasticity
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006716
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006716_Neurodevelopmental_Disorder_with_Microcephaly_Cortical_Malformations_and_Spasticity


id: 7543
description: DOID:0111347 epidermolysis bullosa with congenital localized absence of skin and deformity of nails
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111347
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111347_epidermolysis_bullosa_with_congenital_localized_absence_of_skin_and_deformity_of_nails


id: 7545
description: DOID:9005879 Epidermolysis Bullosa Dystrophica Autosomal Recessive Localisata Variant
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005879
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005879_Epidermolysis_Bullosa_Dystrophica_Autosomal_Recessive_Localisata_Variant


id: 7557
description: DOID:9003701 Intellectual Developmental Disorder with Autism and Dysmorphic Facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003701
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003701_Intellectual_Developmental_Disorder_with_Autism_and_Dysmorphic_Facies


id: 7593
description: DOID:0060827 X-linked intellectual disability-psychosis-macroorchidism syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060827
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060827_X-linked_intellectual_disability-psychosis-macroorchidism_syndrome


id: 7602
description: DOID:0070461 mitochondrial complex V (ATP synthase) deficiency nuclear type 4A
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070461
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070461_mitochondrial_complex_V_(ATP_synthase)_deficiency_nuclear_type_4A


id: 7603
description: DOID:0070462 mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070462
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070462_mitochondrial_complex_V_(ATP_synthase)_deficiency_nuclear_type_4B


id: 7616
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002313
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002313_Autosomal_Recessive_Progressive_External_Ophthalmoplegia_with_Mitochondrial_DNA_Deletions_6

description:
  DOID:9002313 Autosomal Recessive Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions 6


id: 7628
description: DOID:9006181 Congenital Muscular Dystrophy with Central Nervous System Involvement
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006181
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006181_Congenital_Muscular_Dystrophy_with_Central_Nervous_System_Involvement


id: 7639
description: DOID:9001870 Osteoporosis Childhood- or Juvenile-Onset with Developmental Delay
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001870
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001870_Osteoporosis_Childhood-_or_Juvenile-Onset_with_Developmental_Delay


id: 7658
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080311
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080311_X-linked_mental_retardation_with_cerebellar_hypoplasia_and_distinctive_facial_appearance

description:
  DOID:0080311 X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance


id: 7660
description: DOID:9008147 Cancer Alopecia Pigment Dyscrasia Onychodystrophy and Keratoderma
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008147
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008147_Cancer_Alopecia_Pigment_Dyscrasia_Onychodystrophy_and_Keratoderma


id: 7667
description: DOID:9002417 Pontine Microangiopathy and Leukoencephalopathy Autosomal Dominant
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002417
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002417_Pontine_Microangiopathy_and_Leukoencephalopathy_Autosomal_Dominant


id: 7669
description: DOID:9003529 Hereditary Angiopathy with Nephropathy Aneurysms and Muscle Cramps
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003529
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003529_Hereditary_Angiopathy_with_Nephropathy_Aneurysms_and_Muscle_Cramps


id: 7701
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004548
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004548_Neurodevelopmental_Disorder_with_Progressive_Spasticity_and_Brain_White_Matter_Abnormalities

description:
  DOID:9004548 Neurodevelopmental Disorder with Progressive Spasticity and Brain White Matter Abnormalities


id: 7748
description: DOID:9005566 NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH LARGE EARS AND DYSMORPHIC FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005566
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005566_NEURODEVELOPMENTAL_DISORDER_WITH_POOR_GROWTH_LARGE_EARS_AND_DYSMORPHIC_FACIES


id: 7797
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006288
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006288_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AND_EARLY-ONSET_DOPA-RESPONSIVE_DYSTONIA-PARKINSONISM

description:
  DOID:9006288 INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND EARLY-ONSET DOPA-RESPONSIVE DYSTONIA-PARKINSONISM


id: 7800
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111518
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111518_autosomal_dominant_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_5

description:
  DOID:0111518 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5


id: 7802
description: DOID:9004658 Rod-Cone Dystrophy Sensorineural Deafness and Fanconi-Type Renal Dysfunction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004658
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004658_Rod-Cone_Dystrophy_Sensorineural_Deafness_and_Fanconi-Type_Renal_Dysfunction


id: 7804
description: DOID:0070432 hyperphosphatasia with impaired intellectual development syndrome 5
n: 13
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070432
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070432_hyperphosphatasia_with_impaired_intellectual_development_syndrome_5


id: 7811
description: DOID:0070510 inflammatory poikiloderma with hair abnormalities and acral keratoses
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070510
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070510_inflammatory_poikiloderma_with_hair_abnormalities_and_acral_keratoses


id: 7819
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004521
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004521_Intellectual_Developmental_Disorder_with_Behavioral_Abnormalities_and_Craniofacial_Dysmorphism_with_or_without_Seizures

description:
  DOID:9004521 Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures


id: 7843
description: DOID:9000949 DEVELOPMENTAL DELAY INTELLECTUAL DISABILITY OBESITY AND DYSMORPHIC FEATURES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000949
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000949_DEVELOPMENTAL_DELAY_INTELLECTUAL_DISABILITY_OBESITY_AND_DYSMORPHIC_FEATURES


id: 7853
description: DOID:0111666 proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111666
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111666_proliferative_vasculopathy_and_hydranencephaly-hydrocephaly_syndrome


id: 7862
description: DOID:0110639 congenital muscular dystrophy due to integrin alpha-7 deficiency
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0110639
name:
  Disease.RGD_v4_cfa_gskb_DOID:0110639_congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency


id: 7872
description: DOID:9000609 Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000609
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000609_Combined_Cerebellar_and_Peripheral_Ataxia_with_Hearing_Loss_and_Diabetes_Mellitus


id: 7883
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112290
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112290_spondyloepiphyseal_dysplasia_sensorineural_hearing_loss_intellectual_developmental_disorder_and_Leber_congenital_amaurosis

description:
  DOID:0112290 spondyloepiphyseal dysplasia sensorineural hearing loss intellectual developmental disorder and Leber congenital amaurosis


id: 7919
description: DOID:9000260 OSTEOCHONDRODYSPLASIA COMPLEX LETHAL SYMOENS-BARNES-GISTELINCK TYPE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000260
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000260_OSTEOCHONDRODYSPLASIA_COMPLEX_LETHAL_SYMOENS-BARNES-GISTELINCK_TYPE


id: 7920
description: DOID:9004939 Leigh Necrotizing Encephalopathy due to Pyruvate Carboxylase Deficiency
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004939
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004939_Leigh_Necrotizing_Encephalopathy_due_to_Pyruvate_Carboxylase_Deficiency


id: 7945
description: DOID:9004131 NEURODEVELOPMENTAL DISORDER WITH SPEECH DELAY AND VARIABLE OCULAR ANOMALIES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004131
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004131_NEURODEVELOPMENTAL_DISORDER_WITH_SPEECH_DELAY_AND_VARIABLE_OCULAR_ANOMALIES


id: 7988
description: DOID:0050997 cerebellar ataxia impaired intellectual development and dysequilibrium syndrome
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0050997
name:
  Disease.RGD_v4_cfa_gskb_DOID:0050997_cerebellar_ataxia_impaired_intellectual_development_and_dysequilibrium_syndrome


id: 7989
description: DOID:0070559 cerebellar ataxia impaired intellectual development and dysequilibrium syndrome 4
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070559
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070559_cerebellar_ataxia_impaired_intellectual_development_and_dysequilibrium_syndrome_4


id: 7998
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007224
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007224_Neurodevelopmental_Disorder_with_Facial_Dysmorphism_Absent_Language_and_Pseudo-Pelger-Huet_Anomaly

description:
  DOID:9007224 Neurodevelopmental Disorder with Facial Dysmorphism Absent Language and Pseudo-Pelger-Huet Anomaly


id: 8002
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003751
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003751_CEREBELLAR_DYSFUNCTION_IMPAIRED_INTELLECTUAL_DEVELOPMENT_AND_HYPOGONADOTROPIC_HYPOGONADISM

description:
  DOID:9003751 CEREBELLAR DYSFUNCTION IMPAIRED INTELLECTUAL DEVELOPMENT AND HYPOGONADOTROPIC HYPOGONADISM


id: 8023
description: DOID:9003434 Congenital Disorder of Glycosylation with Defective Fucosylation 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003434
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003434_Congenital_Disorder_of_Glycosylation_with_Defective_Fucosylation_1


id: 8031
description: DOID:9009244 Microcephaly Facial Dysmorphism Renal Agenesis and Ambiguous Genitalia Syndrome
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009244
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009244_Microcephaly_Facial_Dysmorphism_Renal_Agenesis_and_Ambiguous_Genitalia_Syndrome


id: 8047
description: DOID:9000594 Cataracts Hearing Impairment Nephrotic Syndrome and Enterocolitis 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000594
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000594_Cataracts_Hearing_Impairment_Nephrotic_Syndrome_and_Enterocolitis_1


id: 8049
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006075
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006075_Facial_Dysmorphism_Hypertrichosis_Epilepsy_Intellectual/Developmental_Delay_and_Gingival_Overgrowth_Syndrome

description:
  DOID:9006075 Facial Dysmorphism Hypertrichosis Epilepsy Intellectual/Developmental Delay and Gingival Overgrowth Syndrome


id: 8073
description: DOID:9007560 Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007560
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007560_Neonatal_Severe_Encephalopathy_with_Lactic_Acidosis_and_Brain_Abnormalities


id: 8096
description: DOID:9008128 NEURODEVELOPMENTAL DISORDER WITH MOTOR ABNORMALITIES SEIZURES AND FACIAL DYSMORPHISM
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008128
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008128_NEURODEVELOPMENTAL_DISORDER_WITH_MOTOR_ABNORMALITIES_SEIZURES_AND_FACIAL_DYSMORPHISM


id: 8121
description: DOID:9000512 Neurodevelopmental Disorder with Microcephaly Epilepsy and Hypomyelination
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000512
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000512_Neurodevelopmental_Disorder_with_Microcephaly_Epilepsy_and_Hypomyelination


id: 8150
description: DOID:9006331 Neurodevelopmental Disorder with Microcephaly Impaired Language and Gait Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006331
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006331_Neurodevelopmental_Disorder_with_Microcephaly_Impaired_Language_and_Gait_Abnormalities


id: 8151
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008961
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008961_Neurodevelopmental_Disorder_with_Microcephaly_Impaired_Language_Epilepsy_and_Gait_Abnormalities

description:
  DOID:9008961 Neurodevelopmental Disorder with Microcephaly Impaired Language Epilepsy and Gait Abnormalities


id: 8181
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007324
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007324_NEURODEVELOPMENTAL_DISORDER_WITH_SEVERE_MOTOR_IMPAIRMENT_ABSENT_LANGUAGE_CEREBRAL_HYPOMYELINATION_AND_BRAIN_ATROPHY

description:
  DOID:9007324 NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT ABSENT LANGUAGE CEREBRAL HYPOMYELINATION AND BRAIN ATROPHY


id: 8224
description: DOID:9009098 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY SEIZURES AND CORTICAL ATROPHY
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009098
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009098_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_SEIZURES_AND_CORTICAL_ATROPHY


id: 8228
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006333
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006333_Junctional_Epidermolysis_Bullosa_7_with_Interstitial_Lung_Disease_and_Nephrotic_Syndrome

description:
  DOID:9006333 Junctional Epidermolysis Bullosa 7 with Interstitial Lung Disease and Nephrotic Syndrome


id: 8236
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007052
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007052_Mitochondrial_Progressive_Myopathy_with_Congenital_Cataract_Hearing_Loss_and_Developmental_Delay

description:
  DOID:9007052 Mitochondrial Progressive Myopathy with Congenital Cataract Hearing Loss and Developmental Delay


id: 8251
description: DOID:0060331 mitochondrial complex V (ATP synthase) deficiency nuclear type 2
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060331
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060331_mitochondrial_complex_V_(ATP_synthase)_deficiency_nuclear_type_2


id: 8272
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001804
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001804_FETAL_AKINESIA_RESPIRATORY_INSUFFICIENCY_MICROCEPHALY_POLYMICROGYRIA_AND_DYSMORPHIC_FACIES

description:
  DOID:9001804 FETAL AKINESIA RESPIRATORY INSUFFICIENCY MICROCEPHALY POLYMICROGYRIA AND DYSMORPHIC FACIES


id: 8275
description: DOID:9002124 IMMUNODEFICIENCY 100 WITH PULMONARY ALVEOLAR PROTEINOSIS AND HYPOGAMMAGLOBULINEMIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002124
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002124_IMMUNODEFICIENCY_100_WITH_PULMONARY_ALVEOLAR_PROTEINOSIS_AND_HYPOGAMMAGLOBULINEMIA


id: 8276
description: DOID:0070513 neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070513
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070513_neurodevelopmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities


id: 8317
description: DOID:9007711 ichthyosis leukocyte vacuoles alopecia and sclerosing cholangitis
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007711
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007711_ichthyosis_leukocyte_vacuoles_alopecia_and_sclerosing_cholangitis


id: 8334
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002875
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002875_MACROCEPHALY_NEURODEVELOPMENTAL_DELAY_LYMPHOID_HYPERPLASIA_AND_PERSISTENT_FETAL_HEMOGLOBIN

description:
  DOID:9002875 MACROCEPHALY NEURODEVELOPMENTAL DELAY LYMPHOID HYPERPLASIA AND PERSISTENT FETAL HEMOGLOBIN


id: 8338
description: DOID:0081263 neurodevelopmental disorder with microcephaly cataracts and renal abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081263
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081263_neurodevelopmental_disorder_with_microcephaly_cataracts_and_renal_abnormalities


id: 8339
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006140
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006140_Neurodevelopmental_Disorder_with_Progressive_Microcephaly_Spasticity_and_Brain_Anomalies

description:
  DOID:9006140 Neurodevelopmental Disorder with Progressive Microcephaly Spasticity and Brain Anomalies


id: 8355
description: DOID:9002267 Neurodevelopmental Disorder with Structural Brain Anomalies and Dysmorphic Facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002267
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002267_Neurodevelopmental_Disorder_with_Structural_Brain_Anomalies_and_Dysmorphic_Facies


id: 8380
description: DOID:9005133 AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005133
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005133_AICAR_Transformylase_Inosine_Monophosphate_Cyclohydrolase_Deficiency


id: 8386
description: DOID:9003110 LEUKOENCEPHALOPATHY DEVELOPMENTAL DELAY AND EPISODIC NEUROLOGIC REGRESSION SYNDROME
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003110
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003110_LEUKOENCEPHALOPATHY_DEVELOPMENTAL_DELAY_AND_EPISODIC_NEUROLOGIC_REGRESSION_SYNDROME


id: 8404
description: DOID:9000950 Polymicrogyria with or without Vascular-Type Ehlers-Danlos Syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000950
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000950_Polymicrogyria_with_or_without_Vascular-Type_Ehlers-Danlos_Syndrome


id: 8407
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002924
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002924_Hyperkeratotic_Cutaneous_Capillary-Venous_Malformations_Associated_with_Cerebral_Capillary_Malformations

description:
  DOID:9002924 Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations


id: 8460
description: DOID:9002510 Focal Epilepsy with Speech Disorder and with or without Mental Retardation
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002510
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002510_Focal_Epilepsy_with_Speech_Disorder_and_with_or_without_Mental_Retardation


id: 8462
description: DOID:9008626 Spastic Paraplegia 91 Autosomal Dominant with or without Cerebellar Ataxia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008626
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008626_Spastic_Paraplegia_91_Autosomal_Dominant_with_or_without_Cerebellar_Ataxia


id: 8474
description: DOID:9008540 46,XX Sex Reversal with Dysgenesis of Kidneys Adrenals and Lungs
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008540
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008540_46,XX_Sex_Reversal_with_Dysgenesis_of_Kidneys_Adrenals_and_Lungs


id: 8484
description: DOID:9008024 Early-Onset Progressive Encephalopathy with Brain Edema and/or Leukoencephalopathy 1
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008024
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008024_Early-Onset_Progressive_Encephalopathy_with_Brain_Edema_and/or_Leukoencephalopathy_1


id: 8487
description: DOID:9000729 OPTIC ATROPHY-ATAXIA-PERIPHERAL NEUROPATHY-GLOBAL DEVELOPMENTAL DELAY SYNDROME
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000729
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000729_OPTIC_ATROPHY-ATAXIA-PERIPHERAL_NEUROPATHY-GLOBAL_DEVELOPMENTAL_DELAY_SYNDROME


id: 8514
description: DOID:9001167 NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001167
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001167_NEURODEVELOPMENTAL_DISORDER_WITH_CEREBRAL_ATROPHY_AND_VARIABLE_FACIAL_DYSMORPHISM


id: 8531
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005813
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005813_DEVELOPMENTAL_DELAY_WITH_OR_WITHOUT_INTELLECTUAL_IMPAIRMENT_OR_BEHAVIORAL_ABNORMALITIES

description:
  DOID:9005813 DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES


id: 8533
description: DOID:9008363 GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008363
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008363_GLOBAL_DEVELOPMENTAL_DELAY_WITH_OR_WITHOUT_IMPAIRED_INTELLECTUAL_DEVELOPMENT


id: 8564
description: DOID:9001445 Cleft Palate Psychomotor Retardation and Distinctive Facial Features
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001445
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001445_Cleft_Palate_Psychomotor_Retardation_and_Distinctive_Facial_Features


id: 8624
description: DOID:0090012 severe combined immunodeficiency with sensitivity to ionizing radiation
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090012
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090012_severe_combined_immunodeficiency_with_sensitivity_to_ionizing_radiation


id: 8652
description: DOID:9006016 SEIZURES EARLY-ONSET WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006016
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006016_SEIZURES_EARLY-ONSET_WITH_NEURODEGENERATION_AND_BRAIN_CALCIFICATIONS


id: 8670
description: DOID:9009154 Neurodevelopmental Disorder with Poor Language and Loss of Hand Skills
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009154
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009154_Neurodevelopmental_Disorder_with_Poor_Language_and_Loss_of_Hand_Skills


id: 8708
description: DOID:9000967 Scaphocephaly Maxillary Retrusion and Impaired Intellectual Development
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000967
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000967_Scaphocephaly_Maxillary_Retrusion_and_Impaired_Intellectual_Development


id: 8739
description: DOID:9001355 Partial Atrioventricular Septal Defect with Heterotaxy Syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001355
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001355_Partial_Atrioventricular_Septal_Defect_with_Heterotaxy_Syndrome


id: 8749
description: DOID:9005799 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 8
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005799
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005799_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_8


id: 8767
description: DOID:9001213 BLADDER DYSFUNCTION AUTONOMIC WITH IMPAIRED PUPILLARY REFLEX AND SECONDARY CAKUT
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001213
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001213_BLADDER_DYSFUNCTION_AUTONOMIC_WITH_IMPAIRED_PUPILLARY_REFLEX_AND_SECONDARY_CAKUT


id: 8769
description: DOID:9000526 DEVELOPMENTAL DELAY IMPAIRED SPEECH AND BEHAVIORAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000526
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000526_DEVELOPMENTAL_DELAY_IMPAIRED_SPEECH_AND_BEHAVIORAL_ABNORMALITIES


id: 8792
description: DOID:9000188 HYPERMETABOLISM DUE TO UNCOUPLED MITOCHONDRIAL OXIDATIVE PHOSPHORYLATION 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000188
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000188_HYPERMETABOLISM_DUE_TO_UNCOUPLED_MITOCHONDRIAL_OXIDATIVE_PHOSPHORYLATION_2


id: 8801
description: DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060740
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060740_methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency


id: 8825
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002421
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002421_Autosomal_Recessive_Peripheral_Neuropathy_with_or_without_Impaired_Intellectual_Development

description:
  DOID:9002421 Autosomal Recessive Peripheral Neuropathy with or without Impaired Intellectual Development


id: 8879
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004115
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004115_NEURODEVELOPMENTAL_DISORDER_WITH_HYPERKINETIC_MOVEMENTS_SEIZURES_AND_STRUCTURAL_BRAIN_ABNORMALITIES

description:
  DOID:9004115 NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS SEIZURES AND STRUCTURAL BRAIN ABNORMALITIES


id: 8913
description: DOID:9008994 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY SHORT STATURE AND SPEECH DELAY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008994
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008994_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_SHORT_STATURE_AND_SPEECH_DELAY


id: 8914
description: DOID:0111859 midface hypoplasia hearing impairment elliptocytosis and nephrocalcinosis
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111859
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111859_midface_hypoplasia_hearing_impairment_elliptocytosis_and_nephrocalcinosis


id: 8929
description: DOID:9000420 Short Stature Amelogenesis Imperfecta and Skeletal Dysplasia with Scoliosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000420
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000420_Short_Stature_Amelogenesis_Imperfecta_and_Skeletal_Dysplasia_with_Scoliosis


id: 8964
description: DOID:9009048 Hyperandrogenism Nonclassic Type due to 21-Hydroxylase Deficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009048
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009048_Hyperandrogenism_Nonclassic_Type_due_to_21-Hydroxylase_Deficiency


id: 8983
description: DOID:0070443 neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070443
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070443_neurodevelopmental_disorder_with_cerebellar_atrophy_and_motor_dysfunction


id: 8996
description: DOID:0070345 vertebral anomalies and variable endocrine and T-cell dysfunction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070345
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070345_vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction


id: 9010
description: DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070436
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070436_hyperphosphatasia_with_impaired_intellectual_development_syndrome_4


id: 9033
description: DOID:9008601 Neurodevelopmental Disorder with Hypotonia Microcephaly and Seizures
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008601
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008601_Neurodevelopmental_Disorder_with_Hypotonia_Microcephaly_and_Seizures


id: 9054
description: DOID:9002854 Noonan Syndrome-Like Disorder with or without Juvenile Myelomonocytic Leukemia
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002854
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002854_Noonan_Syndrome-Like_Disorder_with_or_without_Juvenile_Myelomonocytic_Leukemia


id: 9069
description: DOID:9001042 Neurodevelopmental Disorder with Seizures and Brain Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001042
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001042_Neurodevelopmental_Disorder_with_Seizures_and_Brain_Abnormalities


id: 9070
description: DOID:9005415 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005415
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005415_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_BRAIN_ABNORMALITIES


id: 9079
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000628
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000628_Neurodevelopmental_Disorder_with_Growth_Retardation_Dysmorphic_Facies_and_Corpus_Callosum_Abnormalities

description:
  DOID:9000628 Neurodevelopmental Disorder with Growth Retardation Dysmorphic Facies and Corpus Callosum Abnormalities


id: 9082
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111515
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111515_autosomal_recessive_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_2

description:
  DOID:0111515 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2


id: 9090
description: DOID:9005897 NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005897
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005897_NEURODEVELOPMENTAL_DISORDER_WITH_OR_WITHOUT_VARIABLE_BRAIN_ABNORMALITIES


id: 9096
description: DOID:9003047 ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL OCULAR AND BRAIN ANOMALIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003047
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003047_ECTODERMAL_DYSPLASIA_WITH_FACIAL_DYSMORPHISM_AND_ACRAL_OCULAR_AND_BRAIN_ANOMALIES


id: 9103
description: DOID:9003818 NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003818
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003818_NEURODEVELOPMENTAL_DISORDER_WITH_VISUAL_DEFECTS_AND_BRAIN_ANOMALIES


id: 9167
description: DOID:9003013 Neurodevelopmental Disorder with Alopecia and Brain Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003013
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003013_Neurodevelopmental_Disorder_with_Alopecia_and_Brain_Abnormalities


id: 9177
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111523
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111523_autosomal_recessive_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_3

description:
  DOID:0111523 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3


id: 9180
description: DOID:9003258 CEREBELLAR ATAXIA BRAIN ABNORMALITIES AND CARDIAC CONDUCTION DEFECTS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003258
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003258_CEREBELLAR_ATAXIA_BRAIN_ABNORMALITIES_AND_CARDIAC_CONDUCTION_DEFECTS


id: 9245
description: DOID:9005790 Intellectual Developmental Disorder Autosomal Dominant FRA12A Type
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005790
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005790_Intellectual_Developmental_Disorder_Autosomal_Dominant_FRA12A_Type


id: 9285
description: DOID:9005464 Developmental Delay Language Impairment and Ocular Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005464
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005464_Developmental_Delay_Language_Impairment_and_Ocular_Abnormalities


id: 9294
description: DOID:9008938 Microcornea Rod-Cone Dystrophy Cataract and Posterior Staphyloma 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008938
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008938_Microcornea_Rod-Cone_Dystrophy_Cataract_and_Posterior_Staphyloma_1


id: 9299
description: DOID:9007229 Neurodevelopmental Disorder with Dysmorphic Facies and Variable Seizures
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007229
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007229_Neurodevelopmental_Disorder_with_Dysmorphic_Facies_and_Variable_Seizures


id: 9300
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081266
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081266_pachygyria_microcephaly_developmental_delay_and_dysmorphic_facies_with_or_without_seizures

description:
  DOID:0081266 pachygyria microcephaly developmental delay and dysmorphic facies with or without seizures


id: 9347
description: DOID:9005771 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 7
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005771
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005771_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_7


id: 9406
description: DOID:9001022 Congenital Disorder of Glycosylation with Defective Fucosylation
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001022
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001022_Congenital_Disorder_of_Glycosylation_with_Defective_Fucosylation


id: 9407
description: DOID:9001746 Congenital Disorder of Glycosylation with Defective Fucosylation 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001746
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001746_Congenital_Disorder_of_Glycosylation_with_Defective_Fucosylation_2


id: 9415
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005714
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005714_NEURODEVELOPMENTAL_DISORDER_WITH_IMPAIRED_LANGUAGE_AND_ATAXIA_AND_WITH_OR_WITHOUT_SEIZURES

description:
  DOID:9005714 NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES


id: 9417
description: DOID:9001399 Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001399
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001399_Intellectual_Developmental_Disorder_with_Cardiac_Defects_and_Dysmorphic_Facies


id: 9418
description: DOID:9000999 Infantile Hypotonia with Psychomotor Retardation and Characteristic Facies 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000999
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000999_Infantile_Hypotonia_with_Psychomotor_Retardation_and_Characteristic_Facies_2


id: 9419
description: DOID:9006603 Infantile Hypotonia with Psychomotor Retardation and Characteristic Facies
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006603
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006603_Infantile_Hypotonia_with_Psychomotor_Retardation_and_Characteristic_Facies


id: 9459
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005433
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005433_NEURODEVELOPMENTAL_DISORDER_AND_STRUCTURAL_BRAIN_ANOMALIES_WITH_OR_WITHOUT_SEIZURES_AND_SPASTICITY

description:
  DOID:9005433 NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY


id: 9488
description: DOID:9000683 Distal Renal Tubular Acidosis 2 with Progressive Nerve Deafness
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000683
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000683_Distal_Renal_Tubular_Acidosis_2_with_Progressive_Nerve_Deafness


id: 9500
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001244
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001244_Myopathy_with_Myalgia_increased_Serum_Creatine_Kinase_and_with_or_without_Episodic_Rhabdomyolysis

description:
  DOID:9001244 Myopathy with Myalgia increased Serum Creatine Kinase and with or without Episodic Rhabdomyolysis


id: 9534
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007317
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007317_NEURODEVELOPMENTAL_DISORDER_WITH_OR_WITHOUT_VARIABLE_MOVEMENT_OR_BEHAVIORAL_ABNORMALITIES

description:
  DOID:9007317 NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE MOVEMENT OR BEHAVIORAL ABNORMALITIES


id: 9542
description: DOID:0081321 contractures pterygia and spondylocarpotarsal fusion syndrome 1A
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081321
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081321_contractures_pterygia_and_spondylocarpotarsal_fusion_syndrome_1A


id: 9572
description: DOID:0090007 immunodeficiency-centromeric instability-facial anomalies syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0090007
name:
  Disease.RGD_v4_cfa_gskb_DOID:0090007_immunodeficiency-centromeric_instability-facial_anomalies_syndrome


id: 9586
description: DOID:9000068 X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000068
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000068_X-linked_Spondyloepimetaphyseal_Dysplasia_with_Hypomyelinating_Leukodystrophy


id: 9609
description: DOID:0112012 X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112012
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112012_X-linked_mutilating_palmoplantar_keratoderma_with_periorificial_keratotic_plaques


id: 9613
description: DOID:9009124 NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009124
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009124_NEURODEVELOPMENTAL_DISORDER_WITH_OR_WITHOUT_SEIZURES_AND_GAIT_ABNORMALITIES


id: 9620
description: DOID:9007064 Spondyloepimetaphyseal Dysplasia Borochowitz-Cormier-Daire Type
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007064
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007064_Spondyloepimetaphyseal_Dysplasia_Borochowitz-Cormier-Daire_Type


id: 9663
description: DOID:9001449 Congenital Central Hypoventilation Syndrome 2 and Autonomic Dysfunction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001449
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001449_Congenital_Central_Hypoventilation_Syndrome_2_and_Autonomic_Dysfunction


id: 9710
description: DOID:9005186 RESPIRATORY INFECTIONS RECURRENT AND FAILURE TO THRIVE WITH OR WITHOUT DIARRHEA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005186
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005186_RESPIRATORY_INFECTIONS_RECURRENT_AND_FAILURE_TO_THRIVE_WITH_OR_WITHOUT_DIARRHEA


id: 9766
description: DOID:9005728 Posterior Polar Cataract 11 with Microphthalmia and Neurodevelopmental Abnormalities
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005728
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005728_Posterior_Polar_Cataract_11_with_Microphthalmia_and_Neurodevelopmental_Abnormalities


id: 9768
description: DOID:9005439 Congenital Deafness with Inner Ear Agenesis Microtia and Microdontia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005439
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005439_Congenital_Deafness_with_Inner_Ear_Agenesis_Microtia_and_Microdontia


id: 9773
description: DOID:0111543 juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111543
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111543_juvenile_polyposis-hereditary_hemorrhagic_telangiectasia_syndrome


id: 9788
description: DOID:0111262 infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111262
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111262_infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly


id: 9809
description: DOID:9006720 CONGENITAL SMOOTH MUSCLE HAMARTOMA WITH OR WITHOUT HEMIHYPERTROPHY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006720
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006720_CONGENITAL_SMOOTH_MUSCLE_HAMARTOMA_WITH_OR_WITHOUT_HEMIHYPERTROPHY


id: 9815
description: DOID:0081324 neurodevelopmental disorder with poor growth spastic tetraplegia and hearing loss
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081324
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081324_neurodevelopmental_disorder_with_poor_growth_spastic_tetraplegia_and_hearing_loss


id: 9823
description: DOID:9004467 Neurodevelopmental Disorder with Microcephaly Cerebral Atrophy and Visual Impairment
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004467
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004467_Neurodevelopmental_Disorder_with_Microcephaly_Cerebral_Atrophy_and_Visual_Impairment


id: 9840
description: DOID:0070558 cerebellar ataxia impaired intellectual development and dysequilibrium syndrome 3
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070558
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070558_cerebellar_ataxia_impaired_intellectual_development_and_dysequilibrium_syndrome_3


id: 9868
description: DOID:9005516 Infantile-Onset Multisystem Neurologic Endocrine and Pancreatic Disease 1
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005516
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005516_Infantile-Onset_Multisystem_Neurologic_Endocrine_and_Pancreatic_Disease_1


id: 9875
description: DOID:9003065 Alzheimer's Disease Familial 3 with Spastic Paraparesis and Apraxia
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003065
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003065_Alzheimer's_Disease_Familial_3_with_Spastic_Paraparesis_and_Apraxia


id: 9878
description: DOID:9006129 Alzheimer's Disease Familial 3 with Spastic Paraparesis and Unusual Plaques
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006129
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006129_Alzheimer's_Disease_Familial_3_with_Spastic_Paraparesis_and_Unusual_Plaques


id: 9880
description: DOID:9006712 ICHTHYOTIC KERATODERMA SPASTICITY HYPOMYELINATION AND DYSMORPHIC FACIAL FEATURES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006712
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006712_ICHTHYOTIC_KERATODERMA_SPASTICITY_HYPOMYELINATION_AND_DYSMORPHIC_FACIAL_FEATURES


id: 9887
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006574
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006574_NEURODEVELOPMENTAL_DISORDER_WITH_ABSENT_SPEECH_AND_MOVEMENT_AND_BEHAVIORAL_ABNORMALITIES

description:
  DOID:9006574 NEURODEVELOPMENTAL DISORDER WITH ABSENT SPEECH AND MOVEMENT AND BEHAVIORAL ABNORMALITIES


id: 9890
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111519
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111519_autosomal_dominant_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_6

description:
  DOID:0111519 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6


id: 9902
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008585
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008585_Congenital_Myasthenic_Syndrome_with_Facial_Dysmorphism_associated_with_Acetylcholine_Receptor_Deficiency

description:
  DOID:9008585 Congenital Myasthenic Syndrome with Facial Dysmorphism associated with Acetylcholine Receptor Deficiency


id: 9907
description: DOID:0111649 ectodermal dysplasia ectrodactyly and macular dystrophy syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111649
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111649_ectodermal_dysplasia_ectrodactyly_and_macular_dystrophy_syndrome


id: 9915
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111385
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111385_inclusion_body_myopathy_with_early-onset_Paget_disease_of_bone_with_or_without_frontotemporal_dementia_1

description:
  DOID:0111385 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1


id: 9932
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009115
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009115_Neurodevelopmental_Disorder_with_or_without_Hyperkinetic_Movements_and_Seizures_Autosomal_Recessive

description:
  DOID:9009115 Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures Autosomal Recessive


id: 9968
description: DOID:9001593 Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001593
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001593_Congenital_Keratoconjunctivitis_Sicca_and_Ichthyosiform_Dermatosis


id: 9976
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003689
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003689_HYPOTONIA_HYPERVENTILATION_IMPAIRED_INTELLECTUAL_DEVELOPMENT_DYSAUTONOMIA_EPILEPSY_AND_EYE_ABNORMALITIES

description:
  DOID:9003689 HYPOTONIA HYPERVENTILATION IMPAIRED INTELLECTUAL DEVELOPMENT DYSAUTONOMIA EPILEPSY AND EYE ABNORMALITIES


id: 9978
description: DOID:9008346 SPASTIC PARAPLEGIA INTELLECTUAL DISABILITY NYSTAGMUS AND OBESITY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008346
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008346_SPASTIC_PARAPLEGIA_INTELLECTUAL_DISABILITY_NYSTAGMUS_AND_OBESITY


id: 9980
description: DOID:9006418 NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES ABSENT SPEECH AND HYPOTONIA
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006418
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006418_NEURODEVELOPMENTAL_DISORDER_WITH_BEHAVIORAL_ABNORMALITIES_ABSENT_SPEECH_AND_HYPOTONIA


id: 9981
description: DOID:9009239 Intellectual Developmental Disorder with Macrocephaly Seizures and Speech Delay
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009239
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009239_Intellectual_Developmental_Disorder_with_Macrocephaly_Seizures_and_Speech_Delay


id: 9989
description: DOID:0111591 congenital heart defects hamartomas of tongue and polysyndactyly
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111591
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111591_congenital_heart_defects_hamartomas_of_tongue_and_polysyndactyly


id: 9992
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080209
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080209_sideroblastic_anemia_with_B-cell_immunodeficiency_periodic_fevers_and_developmental_delay

description:
  DOID:0080209 sideroblastic anemia with B-cell immunodeficiency periodic fevers and developmental delay


id: 10033
description: DOID:9005824 X-Linked Hydrocephalus with Congenital Idiopathic Intestinal Pseudoobstruction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005824
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005824_X-Linked_Hydrocephalus_with_Congenital_Idiopathic_Intestinal_Pseudoobstruction


id: 10084
description: DOID:0111331 intellectual disability-severe speech delay-mild dysmorphism syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111331
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111331_intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome


id: 10091
description: DOID:9002745 Short Stature Brachydactyly Intellectual Developmental Disability and Seizures
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002745
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002745_Short_Stature_Brachydactyly_Intellectual_Developmental_Disability_and_Seizures


id: 10095
description: DOID:0081276 cerebellar atrophy visual impairment and psychomotor retardation
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081276
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081276_cerebellar_atrophy_visual_impairment_and_psychomotor_retardation


id: 10173
description: DOID:0080197 congenital muscular dystrophy with cataracts and intellectual disability
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080197
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080197_congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability


id: 10180
description: DOID:9002685 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 4
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002685
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002685_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_4


id: 10182
description: DOID:9004044 Carpal Synostosis with Dysplastic Elbow Joints and Brachydactyly
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004044
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004044_Carpal_Synostosis_with_Dysplastic_Elbow_Joints_and_Brachydactyly


id: 10190
description: DOID:9004901 INTELLECTUAL DISABILITY ANTERIOR MAXILLARY PROTRUSION AND STRABISMUS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004901
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004901_INTELLECTUAL_DISABILITY_ANTERIOR_MAXILLARY_PROTRUSION_AND_STRABISMUS


id: 10199
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003499
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003499_SHORT_STATURE_IMPAIRED_INTELLECTUAL_DEVELOPMENT_MICROCEPHALY_HYPOTONIA_AND_OCULAR_ANOMALIES

description:
  DOID:9003499 SHORT STATURE IMPAIRED INTELLECTUAL DEVELOPMENT MICROCEPHALY HYPOTONIA AND OCULAR ANOMALIES


id: 10258
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006344
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006344_Neurodevelopmental_Disorder_and_Language_Delay_with_or_Without_Structural_Brain_Abnormalities

description:
  DOID:9006344 Neurodevelopmental Disorder and Language Delay with or Without Structural Brain Abnormalities


id: 10259
description: DOID:9006484 Hypomyelination with Brainstem and Spinal Cord Involvement and Leg Spasticity
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006484
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006484_Hypomyelination_with_Brainstem_and_Spinal_Cord_Involvement_and_Leg_Spasticity


id: 10281
description: DOID:9002651 T-CELL LYMPHOPENIA INFANTILE WITH OR WITHOUT NAIL DYSTROPHY AUTOSOMAL DOMINANT
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002651
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002651_T-CELL_LYMPHOPENIA_INFANTILE_WITH_OR_WITHOUT_NAIL_DYSTROPHY_AUTOSOMAL_DOMINANT


id: 10295
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002301
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002301_Childhood-onset_Neurodegeneration_with_Hypotonia_Respiratory_Insufficiency_and_Brain_Imaging_Abnormalities

description:
  DOID:9002301 Childhood-onset Neurodegeneration with Hypotonia Respiratory Insufficiency and Brain Imaging Abnormalities


id: 10321
description: DOID:9006616 Congenital Hydrocephalus 2 with or without Brain or Eye Anomalies
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006616
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006616_Congenital_Hydrocephalus_2_with_or_without_Brain_or_Eye_Anomalies


id: 10332
description: DOID:9007742 B-Cell Immunodeficiency Distal Limb Anomalies and Urogenital Malformations
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007742
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007742_B-Cell_Immunodeficiency_Distal_Limb_Anomalies_and_Urogenital_Malformations


id: 10333
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070050
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070050_neurodevelopmental_disorder_with_hypotonia_stereotypic_hand_movements_and_impaired_language

description:
  DOID:0070050 neurodevelopmental disorder with hypotonia stereotypic hand movements and impaired language


id: 10357
description: DOID:9000463 Neurodevelopmental Disorder with Seizures and Speech and Walking Impairment
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000463
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000463_Neurodevelopmental_Disorder_with_Seizures_and_Speech_and_Walking_Impairment


id: 10361
description: DOID:9009231 Spinocerebellar Ataxia 42 Early-Onset Severe with Neurodevelopmental Deficits
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009231
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009231_Spinocerebellar_Ataxia_42_Early-Onset_Severe_with_Neurodevelopmental_Deficits


id: 10376
description: DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070435
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070435_hyperphosphatasia_with_impaired_intellectual_development_syndrome_3


id: 10381
description: DOID:9000714 COLOBOMA OSTEOPETROSIS MICROPHTHALMIA MACROCEPHALY ALBINISM AND DEAFNESS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000714
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000714_COLOBOMA_OSTEOPETROSIS_MICROPHTHALMIA_MACROCEPHALY_ALBINISM_AND_DEAFNESS


id: 10388
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002794
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002794_NEURODEVELOPMENTAL_DISORDER_WITH_BRAIN_ANOMALIES_AND_WITH_OR_WITHOUT_VERTEBRAL_OR_CARDIAC_ANOMALIES

description:
  DOID:9002794 NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES


id: 10426
description: DOID:9008447 ENCEPHALOPATHY PROGRESSIVE EARLY-ONSET WITH BRAIN ATROPHY AND SPASTICITY
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008447
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008447_ENCEPHALOPATHY_PROGRESSIVE_EARLY-ONSET_WITH_BRAIN_ATROPHY_AND_SPASTICITY


id: 10431
description: DOID:9001360 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001360
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001360_Palmoplantar_Hyperkeratosis_with_Squamous_Cell_Carcinoma_of_Skin_and_Sex_Reversal


id: 10438
description: DOID:9003081 Growth Retardation Developmental Delay Coarse Facies and Early Death
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003081
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003081_Growth_Retardation_Developmental_Delay_Coarse_Facies_and_Early_Death


id: 10476
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112359
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112359_congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss_abnormal_ears_or_developmental_delay

description:
  DOID:0112359 congenital anomalies of kidney and urinary tract syndrome with or without hearing loss abnormal ears or developmental delay


id: 10498
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004675
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004675_Short_Stature_Facial_Dysmorphism_and_Skeletal_Anomalies_with_or_without_Cardiac_Anomalies

description:
  DOID:9004675 Short Stature Facial Dysmorphism and Skeletal Anomalies with or without Cardiac Anomalies


id: 10500
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009129
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009129_Short_Stature_Facial_Dysmorphism_and_Skeletal_Anomalies_with_or_without_Cardiac_Anomalies_1

description:
  DOID:9009129 Short Stature Facial Dysmorphism and Skeletal Anomalies with or without Cardiac Anomalies 1


id: 10557
description: DOID:9006518 DEVELOPMENTAL DELAY BEHAVIORAL ABNORMALITIES AND NEUROPSYCHIATRIC DISORDERS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006518
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006518_DEVELOPMENTAL_DELAY_BEHAVIORAL_ABNORMALITIES_AND_NEUROPSYCHIATRIC_DISORDERS


id: 10563
description: DOID:9008248 Congenital Facial Palsy with Ptosis and Velopharyngeal Dysfunction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008248
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008248_Congenital_Facial_Palsy_with_Ptosis_and_Velopharyngeal_Dysfunction


id: 10586
description: DOID:0080523 adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080523
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080523_adult-onset_leukoencephalopathy_with_axonal_spheroids_and_pigmented_glia


id: 10624
description: DOID:9000368 Gastrointestinal Ulceration Recurrent with Dysfunctional Platelets
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000368
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000368_Gastrointestinal_Ulceration_Recurrent_with_Dysfunctional_Platelets


id: 10682
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112358
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112358_short_stature_facial_dysmorphism_and_skeletal_anomalies_with_or_without_cardiac_anomalies_2

description:
  DOID:0112358 short stature facial dysmorphism and skeletal anomalies with or without cardiac anomalies 2


id: 10691
description: DOID:9005140 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY ATAXIA AND SEIZURES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005140
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005140_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_ATAXIA_AND_SEIZURES


id: 10715
description: DOID:9003497 Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003497
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003497_Mild_Encephalitis/Encephalopathy_with_Reversible_Myelin_Vacuolization


id: 10729
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004447
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004447_Megalencephaly_with_Thick_Corpus_Callosum_Cerebellar_Atrophy_and_Intellectual_Disability

description:
  DOID:9004447 Megalencephaly with Thick Corpus Callosum Cerebellar Atrophy and Intellectual Disability


id: 10736
description: DOID:9001736 Neurodevelopmental Disorder with Speech Impairment and with or without Seizures
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001736
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001736_Neurodevelopmental_Disorder_with_Speech_Impairment_and_with_or_without_Seizures


id: 10771
description: DOID:9007570 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND MOVEMENT ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007570
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007570_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_AND_MOVEMENT_ABNORMALITIES


id: 10779
description: DOID:9006270 Neurodevelopmental Disorder with Craniofacial Dysmorphism and Skeletal Defects
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006270
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006270_Neurodevelopmental_Disorder_with_Craniofacial_Dysmorphism_and_Skeletal_Defects


id: 10784
description: DOID:9005288 Exocrine Pancreatic Insufficiency Dyserythropoietic Anemia and Calvarial Hyperostosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005288
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005288_Exocrine_Pancreatic_Insufficiency_Dyserythropoietic_Anemia_and_Calvarial_Hyperostosis


id: 10798
description: DOID:9006851 NEURODEVELOPMENTAL DISORDER WITH EARLY-ONSET PARKINSONISM AND BEHAVIORAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006851
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006851_NEURODEVELOPMENTAL_DISORDER_WITH_EARLY-ONSET_PARKINSONISM_AND_BEHAVIORAL_ABNORMALITIES


id: 10805
description: DOID:9003890 X-Linked Thrombocytopenia with or without Dyserythropoietic Anemia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003890
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003890_X-Linked_Thrombocytopenia_with_or_without_Dyserythropoietic_Anemia


id: 10811
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003289
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003289_NEURODEVELOPMENTAL_DISORDER_WITH_SEIZURES_SPASTICITY_AND_COMPLETE_OR_PARTIAL_AGENESIS_OF_THE_CORPUS_CALLOSUM

description:
  DOID:9003289 NEURODEVELOPMENTAL DISORDER WITH SEIZURES SPASTICITY AND COMPLETE OR PARTIAL AGENESIS OF THE CORPUS CALLOSUM


id: 10824
description: DOID:9002516 NEURODEVELOPMENTAL DISORDER NONPROGRESSIVE WITH SPASTICITY AND TRANSIENT OPISTHOTONUS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002516
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002516_NEURODEVELOPMENTAL_DISORDER_NONPROGRESSIVE_WITH_SPASTICITY_AND_TRANSIENT_OPISTHOTONUS


id: 10839
description: DOID:9005701 GROWTH RESTRICTION HYPOPLASTIC KIDNEYS ALOPECIA AND DISTINCTIVE FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005701
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005701_GROWTH_RESTRICTION_HYPOPLASTIC_KIDNEYS_ALOPECIA_AND_DISTINCTIVE_FACIES


id: 10842
description: DOID:9005238 NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND ISCHIOPUBIC HYPOPLASIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005238
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005238_NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES_AND_ISCHIOPUBIC_HYPOPLASIA


id: 10849
description: DOID:9002414 NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002414
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002414_NEURODEVELOPMENTAL-CRANIOFACIAL_SYNDROME_WITH_VARIABLE_RENAL_AND_CARDIAC_ABNORMALITIES


id: 10853
description: DOID:0081051 microcephaly growth deficiency seizures and brain malformations
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081051
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081051_microcephaly_growth_deficiency_seizures_and_brain_malformations


id: 10866
description: DOID:9002095 NEURODEVELOPMENTAL DISORDER WITH MOTOR AND SPEECH DELAY AND BEHAVIORAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002095
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002095_NEURODEVELOPMENTAL_DISORDER_WITH_MOTOR_AND_SPEECH_DELAY_AND_BEHAVIORAL_ABNORMALITIES


id: 10869
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003923
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003923_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_AND_SPEECH_DELAY_WITH_OR_WITHOUT_BRAIN_ABNORMALITIES

description:
  DOID:9003923 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND SPEECH DELAY WITH OR WITHOUT BRAIN ABNORMALITIES


id: 10874
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005266
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005266_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_DYSMORPHIC_FACIES_AND_SKELETAL_ANOMALIES_WITH_OR_WITHOUT_SEIZURES

description:
  DOID:9005266 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA DYSMORPHIC FACIES AND SKELETAL ANOMALIES WITH OR WITHOUT SEIZURES


id: 10893
description: DOID:9005221 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005221
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005221_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_1


id: 10909
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007390
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007390_Recurrent_Metabolic_Crises_with_Variable_Encephalomyopathic_Features_and_Neurologic_Regression

description:
  DOID:9007390 Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression


id: 10911
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007986
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007986_NEURODEVELOPMENTAL_DISORDER_WITH_MOTOR_REGRESSION_PROGRESSIVE_SPASTIC_PARAPLEGIA_AND_OROMOTOR_DYSFUNCTION

description:
  DOID:9007986 NEURODEVELOPMENTAL DISORDER WITH MOTOR REGRESSION PROGRESSIVE SPASTIC PARAPLEGIA AND OROMOTOR DYSFUNCTION


id: 10912
description: DOID:9006328 AUTOINFLAMMATORY DISEASE MULTISYSTEM WITH IMMUNE DYSREGULATION X-LINKED
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006328
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006328_AUTOINFLAMMATORY_DISEASE_MULTISYSTEM_WITH_IMMUNE_DYSREGULATION_X-LINKED


id: 10915
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000890
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000890_Mitral_Regurgitation_Conductive_Deafness_and_Fusion_of_Cervical_Vertebrae_and_of_Carpal_and_Tarsal_Bones

description:
  DOID:9000890 Mitral Regurgitation Conductive Deafness and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones


id: 10923
description: DOID:9000372 Autosomal Dominant Intellectual Developmental Disorder 63 with Macrocephaly
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000372
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000372_Autosomal_Dominant_Intellectual_Developmental_Disorder_63_with_Macrocephaly


id: 10944
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006049
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006049_NEURODEVELOPMENTAL_DISORDER_WITH_LANGUAGE_DELAY_AND_BEHAVIORAL_ABNORMALITIES_WITH_OR_WITHOUT_SEIZURES

description:
  DOID:9006049 NEURODEVELOPMENTAL DISORDER WITH LANGUAGE DELAY AND BEHAVIORAL ABNORMALITIES WITH OR WITHOUT SEIZURES


id: 10948
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005631
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005631_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SHORT_STATURE_FACIAL_ANOMALIES_AND_SPEECH_DEFECTS

description:
  DOID:9005631 INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE FACIAL ANOMALIES AND SPEECH DEFECTS


id: 10951
description: DOID:9007897 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY SEIZURES AND BRAIN ATROPHY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007897
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007897_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_SEIZURES_AND_BRAIN_ATROPHY


id: 10962
description: DOID:9000305 LEUKOENCEPHALOPATHY PROGRESSIVE INFANTILE-ONSET WITH OR WITHOUT DEAFNESS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000305
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000305_LEUKOENCEPHALOPATHY_PROGRESSIVE_INFANTILE-ONSET_WITH_OR_WITHOUT_DEAFNESS


id: 10963
description: DOID:9004489 DEAFNESS CONGENITAL AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004489
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004489_DEAFNESS_CONGENITAL_AND_ADULT-ONSET_PROGRESSIVE_LEUKOENCEPHALOPATHY


id: 10966
description: DOID:9004721 HYPOPIGMENTATION ORGANOMEGALY AND DELAYED MYELINATION AND DEVELOPMENT
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004721
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004721_HYPOPIGMENTATION_ORGANOMEGALY_AND_DELAYED_MYELINATION_AND_DEVELOPMENT


id: 10968
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003021
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003021_Microcephaly_Cataracts_Impaired_Intellectual_Development_and_Dystonia_with_Abnormal_Striatum

description:
  DOID:9003021 Microcephaly Cataracts Impaired Intellectual Development and Dystonia with Abnormal Striatum


id: 10974
description: DOID:9001114 Immunodeficiency 94 with Autoinflammation and Dysmorphic Facies
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001114
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001114_Immunodeficiency_94_with_Autoinflammation_and_Dysmorphic_Facies


id: 10986
description: DOID:9004411 Atrioventricular Septal Defect and Common Atrioventricular Junction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004411
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004411_Atrioventricular_Septal_Defect_and_Common_Atrioventricular_Junction


id: 11026
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111525
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111525_autosomal_dominant_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_4

description:
  DOID:0111525 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4


id: 11040
description: DOID:0050813 spondyloepiphyseal dysplasia with congenital joint dislocations
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0050813
name:
  Disease.RGD_v4_cfa_gskb_DOID:0050813_spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations


id: 11050
description: DOID:9007464 Proximal Renal Tubular Acidosis with Ocular Abnormalities and Mental Retardation
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007464
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007464_Proximal_Renal_Tubular_Acidosis_with_Ocular_Abnormalities_and_Mental_Retardation


id: 11060
description: DOID:0060349 microcephaly with or without chorioretinopathy lymphedema or mental retardation
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060349
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060349_microcephaly_with_or_without_chorioretinopathy_lymphedema_or_mental_retardation


id: 11061
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080327
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080327_multinucleated_neurons_anhydramnios_renal_dysplasia_cerebellar_hypoplasia_and_hydranencephaly

description:
  DOID:0080327 multinucleated neurons anhydramnios renal dysplasia cerebellar hypoplasia and hydranencephaly


id: 11081
description: DOID:9000682 Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000682
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000682_Craniofacial_Anomalies_and_Anterior_Segment_Dysgenesis_Syndrome


id: 11104
description: DOID:0060828 X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060828
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060828_X-linked_intellectual_disability-cardiomegaly-congestive_heart_failure_syndrome


id: 11125
description: DOID:0111333 early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111333
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111333_early-onset_myopathy-areflexia-respiratory_distress-dysphagia_syndrome


id: 11151
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001346
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001346_Hereditary_Fibrosing_Poikiloderma_with_Tendon_Contractures_Myopathy_and_Pulmonary_Fibrosis

description:
  DOID:9001346 Hereditary Fibrosing Poikiloderma with Tendon Contractures Myopathy and Pulmonary Fibrosis


id: 11162
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081301
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081301_intellectual_developmental_disorder_with_ocular_anomalies_and_distinctive_facial_features

description:
  DOID:0081301 intellectual developmental disorder with ocular anomalies and distinctive facial features


id: 11186
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009214
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009214_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SPEECH_DELAY_DYSMORPHIC_FACIES_AND_T-CELL_ABNORMALITIES

description:
  DOID:9009214 INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY DYSMORPHIC FACIES AND T-CELL ABNORMALITIES


id: 11190
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009123
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009123_Neurodevelopmental_Disorder_with_Movement_Abnormalities_Abnormal_Gait_and_Autistic_Features

description:
  DOID:9009123 Neurodevelopmental Disorder with Movement Abnormalities Abnormal Gait and Autistic Features


id: 11233
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081396
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081396_neonatal_lethal_pontocerebellar_hypoplasia_hypotonia_and_respiratory_insufficiency_syndrome

description:
  DOID:0081396 neonatal lethal pontocerebellar hypoplasia hypotonia and respiratory insufficiency syndrome


id: 11250
description: DOID:9005606 Global Developmental Delay Lung Cysts Overgrowth and Wilms Tumor
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005606
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005606_Global_Developmental_Delay_Lung_Cysts_Overgrowth_and_Wilms_Tumor


id: 11252
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008698
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008698_NEURODEVELOPMENTAL_DISORDER_WITH_GAIT_DISTURBANCE_DYSMORPHIC_FACIES_AND_BEHAVIORAL_ABNORMALITIES_X-LINKED

description:
  DOID:9008698 NEURODEVELOPMENTAL DISORDER WITH GAIT DISTURBANCE DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES X-LINKED


id: 11265
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081387
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081387_neurodevelopmental_disorder_with_motor_and_language_delay_ocular_defects_and_brain_abnormalities

description:
  DOID:0081387 neurodevelopmental disorder with motor and language delay ocular defects and brain abnormalities


id: 11280
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008751
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008751_NEURODEVELOPMENTAL_DISORDER_WITH_CHARACTERISTIC_FACIAL_AND_ECTODERMAL_FEATURES_AND_TETRAPARESIS_1

description:
  DOID:9008751 NEURODEVELOPMENTAL DISORDER WITH CHARACTERISTIC FACIAL AND ECTODERMAL FEATURES AND TETRAPARESIS 1


id: 11282
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004088
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004088_NEURODEVELOPMENTAL_DISORDER_WITH_INTENTION_TREMOR_PYRAMIDAL_SIGNS_DYSPRAXIA_AND_OCULAR_ANOMALIES

description:
  DOID:9004088 NEURODEVELOPMENTAL DISORDER WITH INTENTION TREMOR PYRAMIDAL SIGNS DYSPRAXIA AND OCULAR ANOMALIES


id: 11300
description: DOID:9000652 Cardiac Conduction Disease with or without Dilated Cardiomyopathy
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000652
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000652_Cardiac_Conduction_Disease_with_or_without_Dilated_Cardiomyopathy


id: 11312
description: DOID:0070437 hyperphosphatasia with impaired intellectual development syndrome 6
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070437
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070437_hyperphosphatasia_with_impaired_intellectual_development_syndrome_6


id: 11315
description: DOID:9003272 ENCEPHALITIS ACUTE INFECTION (VIRAL)-INDUCED SUSCEPTIBILITY TO 11
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003272
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003272_ENCEPHALITIS_ACUTE_INFECTION_(VIRAL)-INDUCED_SUSCEPTIBILITY_TO_11


id: 11316
description: DOID:9009076 XEROSIS AND GROWTH FAILURE WITH IMMUNE AND PULMONARY DYSFUNCTION SYNDROME
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009076
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009076_XEROSIS_AND_GROWTH_FAILURE_WITH_IMMUNE_AND_PULMONARY_DYSFUNCTION_SYNDROME


id: 11329
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002540
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002540_Mitochondrial_Neurodevelopmental_Disorder_with_Abnormal_Movements_and_Lactic_Acidosis_with_or_without_Seizures

description:
  DOID:9002540 Mitochondrial Neurodevelopmental Disorder with Abnormal Movements and Lactic Acidosis with or without Seizures


id: 11330
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004450
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004450_Thiamine_Metabolism_Dysfunction_Syndrome_4_(Bilateral_Striatal_Degeneration_and_Progressive_Polyneuropathy_Type)

description:
  DOID:9004450 Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)


id: 11341
description: DOID:0081419 childhood-onset dystonia with optic atrophy and basal ganglia abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081419
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081419_childhood-onset_dystonia_with_optic_atrophy_and_basal_ganglia_abnormalities


id: 11370
description: DOID:9004026 Dilated Cardiomyopathy with Woolly Hair Keratoderma and Tooth Agenesis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004026
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004026_Dilated_Cardiomyopathy_with_Woolly_Hair_Keratoderma_and_Tooth_Agenesis


id: 11395
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007485
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007485_Severe_Combined_Immunodeficiency_with_Microcephaly_Growth_Retardation_and_Sensitivity_to_Ionizing_Radiation

description:
  DOID:9007485 Severe Combined Immunodeficiency with Microcephaly Growth Retardation and Sensitivity to Ionizing Radiation


id: 11425
description: DOID:0080837 growth hormone insensitivity syndrome with immune dysregulation 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080837
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080837_growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2


id: 11438
description: DOID:0111645 Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111645
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111645_Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome


id: 11439
description: DOID:0070469 neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070469
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070469_neurodevelopmental_disorder_with_dysmorphic_facies_and_thin_corpus_callosum


id: 11469
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005477
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005477_Retinal_Dystrophy_Optic_Nerve_Edema_Splenomegaly_Anhidrosis_and_Migraine_Headache_Syndrome

description:
  DOID:9005477 Retinal Dystrophy Optic Nerve Edema Splenomegaly Anhidrosis and Migraine Headache Syndrome


id: 11494
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112247
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112247_congenital_heart_defects_dysmorphic_facial_features_and_intellectual_developmental_disorder

description:
  DOID:0112247 congenital heart defects dysmorphic facial features and intellectual developmental disorder


id: 11526
description: DOID:9000947 INTELLECTUAL DEVELOPMENTAL DISORDER X-LINKED WITH PANHYPOPITUITARISM
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000947
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000947_INTELLECTUAL_DEVELOPMENTAL_DISORDER_X-LINKED_WITH_PANHYPOPITUITARISM


id: 11527
description: DOID:9004048 X-Linked Mental Retardation with Isolated Growth Hormone Deficiency
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004048
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004048_X-Linked_Mental_Retardation_with_Isolated_Growth_Hormone_Deficiency


id: 11546
description: DOID:9002230 GROWTH RETARDATION INTELLECTUAL DEVELOPMENTAL DISORDER HYPOTONIA AND HEPATOPATHY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002230
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002230_GROWTH_RETARDATION_INTELLECTUAL_DEVELOPMENTAL_DISORDER_HYPOTONIA_AND_HEPATOPATHY


id: 11548
description: DOID:9003945 Neurodevelopmental Disorder with Hypotonia Dysmorphic Facies and Skin Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003945
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003945_Neurodevelopmental_Disorder_with_Hypotonia_Dysmorphic_Facies_and_Skin_Abnormalities


id: 11561
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111516
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111516_autosomal_recessive_progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions_4

description:
  DOID:0111516 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4


id: 11563
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002933
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002933_Neurodevelopmental_Disorder_with_Impaired_Intellectual_Development_Hypotonia_and_Ataxia

description:
  DOID:9002933 Neurodevelopmental Disorder with Impaired Intellectual Development Hypotonia and Ataxia


id: 11602
description: DOID:9008370 NEURODEVELOPMENTAL DISORDER WITH ATAXIA HYPOTONIA AND MICROCEPHALY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008370
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008370_NEURODEVELOPMENTAL_DISORDER_WITH_ATAXIA_HYPOTONIA_AND_MICROCEPHALY


id: 11606
description: DOID:0110003 3-methylglutaconic aciduria with cataracts neurologic involvement and neutropenia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0110003
name:
  Disease.RGD_v4_cfa_gskb_DOID:0110003_3-methylglutaconic_aciduria_with_cataracts_neurologic_involvement_and_neutropenia


id: 11613
description: DOID:9003193 Neurodevelopmental Disorder with Central and Peripheral Motor Dysfunction
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003193
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003193_Neurodevelopmental_Disorder_with_Central_and_Peripheral_Motor_Dysfunction


id: 11625
description: DOID:9006936 Anadysplasia-Like Spontaneously Remitting Spondylometaphyseal Dysplasia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006936
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006936_Anadysplasia-Like_Spontaneously_Remitting_Spondylometaphyseal_Dysplasia


id: 11635
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009113
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009113_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_FEEDING_DIFFICULTIES_FACIAL_DYSMORPHISM_AND_BRAIN_ABNORMALITIES

description:
  DOID:9009113 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA FEEDING DIFFICULTIES FACIAL DYSMORPHISM AND BRAIN ABNORMALITIES


id: 11657
description: DOID:0070339 cerebellar hyplasia/atrophy epilepsy and global developmental delay
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070339
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070339_cerebellar_hyplasia/atrophy_epilepsy_and_global_developmental_delay


id: 11662
description: DOID:0070557 cerebellar ataxia impaired intellectual development and dysequilibrium syndrome 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070557
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070557_cerebellar_ataxia_impaired_intellectual_development_and_dysequilibrium_syndrome_2


id: 11694
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004880
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004880_CATARACTS_GROWTH_HORMONE_DEFICIENCY_SENSORY_NEUROPATHY_SENSORINEURAL_HEARING_LOSS_AND_SKELETAL_DYSPLASIA

description:
  DOID:9004880 CATARACTS GROWTH HORMONE DEFICIENCY SENSORY NEUROPATHY SENSORINEURAL HEARING LOSS AND SKELETAL DYSPLASIA


id: 11697
description: DOID:9003089 Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003089
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003089_Autosomal_Dominant_Deafness_39_with_Dentinogenesis_Imperfecta_1


id: 11707
description: DOID:9007909 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CHARACTERISTIC BRAIN ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007909
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007909_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_CHARACTERISTIC_BRAIN_ABNORMALITIES


id: 11713
description: DOID:9001863 PINEAL HYPERPLASIA INSULIN-RESISTANT DIABETES MELLITUS AND SOMATIC ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001863
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001863_PINEAL_HYPERPLASIA_INSULIN-RESISTANT_DIABETES_MELLITUS_AND_SOMATIC_ABNORMALITIES


id: 11714
description: DOID:9006383 Neurodevelopmental Disorder with Seizures Microcephaly and Brain Abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006383
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006383_Neurodevelopmental_Disorder_with_Seizures_Microcephaly_and_Brain_Abnormalities


id: 11719
description: DOID:9000951 Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000951
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000951_Retinal_Arterial_Macroaneurysm_with_Supravalvular_Pulmonic_Stenosis


id: 11739
description: DOID:9006824 46,XY Partial Gonadal Dysgenesis with Minifascicular Neuropathy
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006824
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006824_46,XY_Partial_Gonadal_Dysgenesis_with_Minifascicular_Neuropathy


id: 11763
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001248
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001248_Epidermolysis_Bullosa_Simplex_3_Localized_or_Generalized_Intermediate_with_BP230_Deficiency

description:
  DOID:9001248 Epidermolysis Bullosa Simplex 3 Localized or Generalized Intermediate with BP230 Deficiency


id: 11772
description: DOID:0081048 congenital limbs-face contractures-hypotonia-developmental delay syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081048
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081048_congenital_limbs-face_contractures-hypotonia-developmental_delay_syndrome


id: 11773
description: DOID:9001769 Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9001769
name:
  Disease.RGD_v4_cfa_gskb_DOID:9001769_Intellectual_Disability_with_Episodic_Ataxia_and_Congenital_Arthrogryposis


id: 11774
description: DOID:9008988 Infantile Hypotonia with Psychomotor Retardation and Characteristic Facies 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008988
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008988_Infantile_Hypotonia_with_Psychomotor_Retardation_and_Characteristic_Facies_1


id: 11778
description: DOID:0111194 autosomal dominant adult-onset proximal spinal muscular atrophy
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111194
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111194_autosomal_dominant_adult-onset_proximal_spinal_muscular_atrophy


id: 11788
description: DOID:9004825 Skeletal Dysplasia And Progressive Central Nervous System Degeneration Lethal
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004825
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004825_Skeletal_Dysplasia_And_Progressive_Central_Nervous_System_Degeneration_Lethal


id: 11791
description: DOID:9003344 INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003344
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003344_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_NEUROPSYCHIATRIC_FEATURES


id: 11798
description: DOID:9004695 Intellectual Developmental Disorder with Autism and Speech Delay
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004695
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004695_Intellectual_Developmental_Disorder_with_Autism_and_Speech_Delay


id: 11859
description: DOID:0070556 cerebellar ataxia impaired intellectual development and dysequilibrium syndrome 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070556
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070556_cerebellar_ataxia_impaired_intellectual_development_and_dysequilibrium_syndrome_1


id: 11870
description: DOID:9004230 DEVELOPMENTAL DELAY HYPOTONIA MUSCULOSKELETAL DEFECTS AND BEHAVIORAL ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004230
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004230_DEVELOPMENTAL_DELAY_HYPOTONIA_MUSCULOSKELETAL_DEFECTS_AND_BEHAVIORAL_ABNORMALITIES


id: 11875
description: DOID:9006408 NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MOVEMENT ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006408
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006408_NEURODEVELOPMENTAL_DISORDER_WITH_PROGRESSIVE_MOVEMENT_ABNORMALITIES


id: 11878
description: DOID:0060935 infantile hypotonia with psychomotor retardation and characteristic facies-3
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060935
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060935_infantile_hypotonia_with_psychomotor_retardation_and_characteristic_facies-3


id: 11881
description: DOID:0080312 neurodevelopmental disorder with midbrain and hindbrain malformations
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0080312
name:
  Disease.RGD_v4_cfa_gskb_DOID:0080312_neurodevelopmental_disorder_with_midbrain_and_hindbrain_malformations


id: 11919
description: DOID:9002077 Encephalopathy due to Defective Mitochondrial and Peroxisomal Fission 2
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002077
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002077_Encephalopathy_due_to_Defective_Mitochondrial_and_Peroxisomal_Fission_2


id: 11922
description: DOID:9000572 Hereditary Sensory Neuropathy with Spastic Paraplegia Autosomal Recessive
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000572
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000572_Hereditary_Sensory_Neuropathy_with_Spastic_Paraplegia_Autosomal_Recessive


id: 11926
description: DOID:9005055 NEURODEVELOPMENTAL DISORDER WITH SEIZURES HYPOTONIA AND BRAIN IMAGING ABNORMALITIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005055
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005055_NEURODEVELOPMENTAL_DISORDER_WITH_SEIZURES_HYPOTONIA_AND_BRAIN_IMAGING_ABNORMALITIES


id: 11954
description: DOID:9007371 INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007371
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007371_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_PAROXYSMAL_DYSKINESIA_OR_SEIZURES


id: 11959
description: DOID:9004098 DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL DISABILITY AND DYSMORPHIC FACIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004098
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004098_DEVELOPMENTAL_DELAY_WITH_VARIABLE_INTELLECTUAL_DISABILITY_AND_DYSMORPHIC_FACIES


id: 11966
description: DOID:9006921 CORPUS CALLOSUM AGENESIS OF WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006921
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006921_CORPUS_CALLOSUM_AGENESIS_OF_WITH_FACIAL_ANOMALIES_AND_CEREBELLAR_ATAXIA


id: 12000
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009055
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009055_Combined_Immunodeficiency_and_Megaloblastic_Anemia_with_or_without_Hyperhomocysteinemia

description:
  DOID:9009055 Combined Immunodeficiency and Megaloblastic Anemia with or without Hyperhomocysteinemia


id: 12001
description: DOID:0112061 immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112061
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112061_immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia


id: 12002
description: DOID:0112062 immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112062
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112062_immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia


id: 12003
description: DOID:0112064 immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112064
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112064_immunodeficiency_73a_with_defective_neutrophil_chemotaxis_and_leukocytosis


id: 12017
description: DOID:0111403 mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111403
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111403_mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations


id: 12035
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009173
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009173_Neurodevelopmental_Disorder_with_Spastic_Quadriplegia_and_Brain_Abnormalities_with_or_without_Seizures

description:
  DOID:9009173 Neurodevelopmental Disorder with Spastic Quadriplegia and Brain Abnormalities with or without Seizures


id: 12041
description: DOID:9006351 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006351
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006351_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_AND_STRUCTURAL_BRAIN_ANOMALIES


id: 12056
description: DOID:9006001 Mental Retardation and Distinctive Facial Features with or without Cardiac Defects
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006001
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006001_Mental_Retardation_and_Distinctive_Facial_Features_with_or_without_Cardiac_Defects


id: 12059
description: DOID:9004582 CONGENITAL HEART DEFECTS MULTIPLE TYPES 8 WITH OR WITHOUT HETEROTAXY
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004582
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004582_CONGENITAL_HEART_DEFECTS_MULTIPLE_TYPES_8_WITH_OR_WITHOUT_HETEROTAXY


id: 12060
description: DOID:9000804 Intellectual Developmental Disorder with Seizures and Language Delay
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000804
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000804_Intellectual_Developmental_Disorder_with_Seizures_and_Language_Delay


id: 12062
description: DOID:9006467 INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006467
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006467_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_SEVERE_SPEECH_AND_AMBULATION_DEFECTS


id: 12063
description: DOID:9006901 Early-Onset Progressive Encephalopathy with Brain Edema and/or Leukoencephalopathy
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006901
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006901_Early-Onset_Progressive_Encephalopathy_with_Brain_Edema_and/or_Leukoencephalopathy


id: 12096
description: DOID:9008819 Diabetes Deafness Developmental Delay and Short Stature Syndrome
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008819
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008819_Diabetes_Deafness_Developmental_Delay_and_Short_Stature_Syndrome


id: 12104
description: DOID:0060783 ectrodactyly ectodermal dysplasia and cleft lip-palate syndrome 3
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060783
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060783_ectrodactyly_ectodermal_dysplasia_and_cleft_lip-palate_syndrome_3


id: 12129
description: DOID:9007380 Congenital Erythroderma with Palmoplantar Keratoderma Hypotrichosis and Hyper-IgE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007380
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007380_Congenital_Erythroderma_with_Palmoplantar_Keratoderma_Hypotrichosis_and_Hyper-IgE


id: 12136
description: DOID:9007294 Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007294
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007294_Lymphedema-Distichiasis_Syndrome_with_Renal_Disease_and_Diabetes_Mellitus


id: 12138
description: DOID:0111373 familial progressive hyperpigmentation with or without hypopigmentation
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111373
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111373_familial_progressive_hyperpigmentation_with_or_without_hypopigmentation


id: 12158
description: DOID:0050768 mitochondrial complex V (ATP synthase) deficiency nuclear type 1
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0050768
name:
  Disease.RGD_v4_cfa_gskb_DOID:0050768_mitochondrial_complex_V_(ATP_synthase)_deficiency_nuclear_type_1


id: 12165
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002043
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002043_Childhood-onset_Neurodegeneration_with_Ataxia_Tremor_Optic_Atrophy_and_Cognitive_Decline

description:
  DOID:9002043 Childhood-onset Neurodegeneration with Ataxia Tremor Optic Atrophy and Cognitive Decline


id: 12174
description: DOID:0070543 neurodevelopmental disorder with cardiomyopathy spasticity and brain abnormalities
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070543
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070543_neurodevelopmental_disorder_with_cardiomyopathy_spasticity_and_brain_abnormalities


id: 12193
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008567
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008567_DEVELOPMENTAL_DELAY_IMPAIRED_SPEECH_AND_BEHAVIORAL_ABNORMALITIES_WITH_OR_WITHOUT_SEIZURES

description:
  DOID:9008567 DEVELOPMENTAL DELAY IMPAIRED SPEECH AND BEHAVIORAL ABNORMALITIES WITH OR WITHOUT SEIZURES


id: 12194
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002595
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002595_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_IMPAIRED_SPEECH_AND_BEHAVIORAL_ABNORMALITIES

description:
  DOID:9002595 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA IMPAIRED SPEECH AND BEHAVIORAL ABNORMALITIES


id: 12208
description: DOID:9008257 Multiple Polyps and Recurrent Inflammatory Fibroid Gastrointestinal
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008257
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008257_Multiple_Polyps_and_Recurrent_Inflammatory_Fibroid_Gastrointestinal


id: 12214
description: DOID:9003917 Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003917
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003917_Combined_Immunodeficiency_with_Autoimmunity_and_Spondylometaphyseal_Dysplasia


id: 12216
description: DOID:9003255 Immunodeficiency 99 with Hypogammaglobulinemia and Autoimmune Cytopenias
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003255
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003255_Immunodeficiency_99_with_Hypogammaglobulinemia_and_Autoimmune_Cytopenias


id: 12222
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9005460
name:
  Disease.RGD_v4_cfa_gskb_DOID:9005460_NEURODEVELOPMENTAL_DISORDER_WITH_HYPOTONIA_AND_AUTISTIC_FEATURES_WITH_OR_WITHOUT_HYPERKINETIC_MOVEMENTS

description:
  DOID:9005460 NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS


id: 12223
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0112106
name:
  Disease.RGD_v4_cfa_gskb_DOID:0112106_chondrodysplasia_with_platyspondyly_distinctive_brachydactyly_hydrocephaly_and_microphthalmia

description:
  DOID:0112106 chondrodysplasia with platyspondyly distinctive brachydactyly hydrocephaly and microphthalmia


id: 12243
description: DOID:9008465 SKELETAL DYSPLASIA MILD WITH JOINT LAXITY AND ADVANCED BONE AGE
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9008465
name:
  Disease.RGD_v4_cfa_gskb_DOID:9008465_SKELETAL_DYSPLASIA_MILD_WITH_JOINT_LAXITY_AND_ADVANCED_BONE_AGE


id: 12246
description: DOID:9000195 Ectopia Lentis Spontaneous Filtering Blebs and Craniofacial Dysmorphism
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000195
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000195_Ectopia_Lentis_Spontaneous_Filtering_Blebs_and_Craniofacial_Dysmorphism


id: 12249
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081125
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081125_craniofacial_dysmorphism_skeletal_anomalies_and_impaired_intellectual_development_syndrome_2

description:
  DOID:0081125 craniofacial dysmorphism skeletal anomalies and impaired intellectual development syndrome 2


id: 12285
description: DOID:0060934 neurodevelopmental disorder with microcephaly epilepsy and brain atrophy
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0060934
name:
  Disease.RGD_v4_cfa_gskb_DOID:0060934_neurodevelopmental_disorder_with_microcephaly_epilepsy_and_brain_atrophy


id: 12291
description: DOID:9002502 Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002502
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002502_Hemorrhagic_Destruction_of_the_Brain_Subependymal_Calcification_and_Cataracts


id: 12299
description: DOID:9007119 Pulmonary Fibrosis and/or Bone Marrow Failure Syndrome Telomere-Related 6
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007119
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007119_Pulmonary_Fibrosis_and/or_Bone_Marrow_Failure_Syndrome_Telomere-Related_6


id: 12304
description: DOID:9004468 Neurodevelopmental Disorder with or without Anomalies of the Brain Eye or Heart
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004468
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004468_Neurodevelopmental_Disorder_with_or_without_Anomalies_of_the_Brain_Eye_or_Heart


id: 12308
description: DOID:9004802 Butyrylcholinesterase Deficiency Fluoride-Resistant Japanese Type
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9004802
name:
  Disease.RGD_v4_cfa_gskb_DOID:9004802_Butyrylcholinesterase_Deficiency_Fluoride-Resistant_Japanese_Type


id: 12324
description: DOID:9007082 Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9007082
name:
  Disease.RGD_v4_cfa_gskb_DOID:9007082_Keratosis_Linearis_with_Ichthyosis_Congenita_and_Sclerosing_Keratoderma


id: 12326
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9006871
name:
  Disease.RGD_v4_cfa_gskb_DOID:9006871_BRANCHIAL_ARCH_ABNORMALITIES_CHOANAL_ATRESIA_ATHELIA_HEARING_LOSS_AND_HYPOTHYROIDISM_SYNDROME

description:
  DOID:9006871 BRANCHIAL ARCH ABNORMALITIES CHOANAL ATRESIA ATHELIA HEARING LOSS AND HYPOTHYROIDISM SYNDROME


id: 12367
description: DOID:0070293 primary autosomal recessive microcephaly 2 with or without cortical malformations
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0070293
name:
  Disease.RGD_v4_cfa_gskb_DOID:0070293_primary_autosomal_recessive_microcephaly_2_with_or_without_cortical_malformations


id: 12396
description: DOID:9003030 Short Stature Onychodysplasia Facial Dysmorphism and Hypotrichosis
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9003030
name:
  Disease.RGD_v4_cfa_gskb_DOID:9003030_Short_Stature_Onychodysplasia_Facial_Dysmorphism_and_Hypotrichosis


id: 12408
description: DOID:9000387 NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY SEIZURES AND NEONATAL CHOLESTASIS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000387
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000387_NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY_SEIZURES_AND_NEONATAL_CHOLESTASIS


id: 12409
description: DOID:9000912 Acute Reversible Leukoencephalopathy with Increased Urinary Alpha-ketoglutarate
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9000912
name:
  Disease.RGD_v4_cfa_gskb_DOID:9000912_Acute_Reversible_Leukoencephalopathy_with_Increased_Urinary_Alpha-ketoglutarate


id: 12413
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009163
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009163_ATAXIA_SPASTIC_CHILDHOOD-ONSET_AUTOSOMAL_RECESSIVE_WITH_OPTIC_ATROPHY_AND_MENTAL_RETARDATION

description:
  DOID:9009163 ATAXIA SPASTIC CHILDHOOD-ONSET AUTOSOMAL RECESSIVE WITH OPTIC ATROPHY AND MENTAL RETARDATION


id: 12423
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0111386
name:
  Disease.RGD_v4_cfa_gskb_DOID:0111386_inclusion_body_myopathy_with_early-onset_Paget_disease_of_bone_with_or_without_frontotemporal_dementia_3

description:
  DOID:0111386 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3


id: 12427
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:0081265
name:
  Disease.RGD_v4_cfa_gskb_DOID:0081265_intellectual_developmental_disorder_with_abnormal_behavior_microcephaly_and_short_stature

description:
  DOID:0081265 intellectual developmental disorder with abnormal behavior microcephaly and short stature


id: 12451
description: DOID:9009192 INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9009192
name:
  Disease.RGD_v4_cfa_gskb_DOID:9009192_INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_OR_WITHOUT_EPILEPSY_OR_CEREBELLAR_ATAXIA


id: 12457
description: DOID:9002109 STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=DOID:9002109
name:
  Disease.RGD_v4_cfa_gskb_DOID:9002109_STRUCTURAL_BRAIN_ANOMALIES_WITH_IMPAIRED_INTELLECTUAL_DEVELOPMENT_AND_CRANIOSYNOSTOSIS


id: 12490
description: PW:0000381 multidrug resistance-associated protein mediated transport pathway
n: 5
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000381
name:
  Curated.RGD_v4_cfa_gskb_PW:0000381_multidrug_resistance-associated_protein_mediated_transport_pathway


id: 12506
description: PW:0000970 granulocyte-macrophage colony-stimulating factor signaling pathway
n: 34
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000970
name:
  Curated.RGD_v4_cfa_gskb_PW:0000970_granulocyte-macrophage_colony-stimulating_factor_signaling_pathway


id: 12641
description: PW:0000401 remethylation pathway of homocysteine metabolism-cobalamin independent betaine dependent
n: 7
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000401
name:
  Curated.RGD_v4_cfa_gskb_PW:0000401_remethylation_pathway_of_homocysteine_metabolism-cobalamin_independent_betaine_dependent


id: 12660
description: PW:0000614 altered transforming growth factor-beta Smad dependent signaling pathway
n: 6
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000614
name:
  Curated.RGD_v4_cfa_gskb_PW:0000614_altered_transforming_growth_factor-beta_Smad_dependent_signaling_pathway


id: 12671
description: PW:0002365 mitochondrial neurogastrointestinal encephalopathy syndrome pathway
n: 19
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0002365
name:
  Curated.RGD_v4_cfa_gskb_PW:0002365_mitochondrial_neurogastrointestinal_encephalopathy_syndrome_pathway


id: 12724
description: PW:0002439 congenital hemidysplasia with ichthyosiform erythroderma and limb defects pathway
n: 21
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0002439
name:
  Curated.RGD_v4_cfa_gskb_PW:0002439_congenital_hemidysplasia_with_ichthyosiform_erythroderma_and_limb_defects_pathway


id: 12773
description: PW:0000639 insulin responsive facilitative sugar transporter mediated glucose transport pathway
n: 67
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000639
name:
  Curated.RGD_v4_cfa_gskb_PW:0000639_insulin_responsive_facilitative_sugar_transporter_mediated_glucose_transport_pathway


id: 12780
description: PW:0000842 acetylcholine signaling pathway via nicotinic acetylcholine receptor
n: 24
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000842
name:
  Curated.RGD_v4_cfa_gskb_PW:0000842_acetylcholine_signaling_pathway_via_nicotinic_acetylcholine_receptor


id: 12846
description: PW:0000801 adrenergic beta receptor agonist and beta-blocker pharmacodynamics pathway
n: 49
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000801
name:
  Curated.RGD_v4_cfa_gskb_PW:0000801_adrenergic_beta_receptor_agonist_and_beta-blocker_pharmacodynamics_pathway


id: 12927
description: PW:0000379 endoplasmic reticulum stress -the unfolded protein response pathway
n: 11
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000379
name:
  Curated.RGD_v4_cfa_gskb_PW:0000379_endoplasmic_reticulum_stress_-the_unfolded_protein_response_pathway


id: 12997
description: PW:0000230 G protein mediated signaling pathway via Galpha12/Galpha13 family
n: 5
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000230
name:
  Curated.RGD_v4_cfa_gskb_PW:0000230_G_protein_mediated_signaling_pathway_via_Galpha12/Galpha13_family


id: 12998
description: PW:0000542 adenosine monophosphate-activated protein kinase (AMPK) signaling pathway
n: 20
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000542
name:
  Curated.RGD_v4_cfa_gskb_PW:0000542_adenosine_monophosphate-activated_protein_kinase_(AMPK)_signaling_pathway


id: 13020
description: PW:0000560 facilitative sugar transporter mediated glucose transport pathway
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000560
name:
  Curated.RGD_v4_cfa_gskb_PW:0000560_facilitative_sugar_transporter_mediated_glucose_transport_pathway


id: 13022
n: 5
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000855
name:
  Curated.RGD_v4_cfa_gskb_PW:0000855_acetylcholine_signaling_pathway_via_muscarinic_acetylcholine_receptors_engaging_G_alphaq_protein_family

description:
  PW:0000855 acetylcholine signaling pathway via muscarinic acetylcholine receptors engaging G alphaq protein family


id: 13025
description: PW:0000399 remethylation pathway of homocysteine metabolism-cobalamin dependent
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000399
name:
  Curated.RGD_v4_cfa_gskb_PW:0000399_remethylation_pathway_of_homocysteine_metabolism-cobalamin_dependent


id: 13044
description: PW:0000383 multispecific organic anion transporter mediated transport pathway
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000383
name:
  Curated.RGD_v4_cfa_gskb_PW:0000383_multispecific_organic_anion_transporter_mediated_transport_pathway


id: 13067
description: PW:0000843 acetylcholine signaling pathway via muscarinic acetylcholine receptor
n: 9
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000843
name:
  Curated.RGD_v4_cfa_gskb_PW:0000843_acetylcholine_signaling_pathway_via_muscarinic_acetylcholine_receptor


id: 13079
description: PW:0001091 serotonin signaling pathway via receptors engaging G alphas protein family
n: 10
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0001091
name:
  Curated.RGD_v4_cfa_gskb_PW:0001091_serotonin_signaling_pathway_via_receptors_engaging_G_alphas_protein_family


id: 13096
description: PW:0000351 altered vascular endothelial growth factor signaling pathway involving the main players
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000351
name:
  Curated.RGD_v4_cfa_gskb_PW:0000351_altered_vascular_endothelial_growth_factor_signaling_pathway_involving_the_main_players


id: 13110
description: PW:0000415 proteasome degradation pathway involving cullin-dependent ubiquitin ligases
n: 10
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000415
name:
  Curated.RGD_v4_cfa_gskb_PW:0000415_proteasome_degradation_pathway_involving_cullin-dependent_ubiquitin_ligases


id: 13142
description: PW:0001375 nicotinamide adenine dinucleotide biosynthesis the salvage pathway
n: 7
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0001375
name:
  Curated.RGD_v4_cfa_gskb_PW:0001375_nicotinamide_adenine_dinucleotide_biosynthesis_the_salvage_pathway


id: 13204
description: PW:0000585 orexin/hypocretin signaling pathway via orexin/hypocretin receptor 1
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000585
name:
  Curated.RGD_v4_cfa_gskb_PW:0000585_orexin/hypocretin_signaling_pathway_via_orexin/hypocretin_receptor_1


id: 13205
description: PW:0000586 orexin/hypocretin signaling pathway via orexin/hypocretin receptor 2
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000586
name:
  Curated.RGD_v4_cfa_gskb_PW:0000586_orexin/hypocretin_signaling_pathway_via_orexin/hypocretin_receptor_2


id: 13207
description: PW:0000602 altered extracellular signal-regulated Raf/Mek/Erk signaling pathway
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000602
name:
  Curated.RGD_v4_cfa_gskb_PW:0000602_altered_extracellular_signal-regulated_Raf/Mek/Erk_signaling_pathway


id: 13232
n: 4
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000856
name:
  Curated.RGD_v4_cfa_gskb_PW:0000856_acetylcholine_signaling_pathway_via_muscarinic_acetylcholine_receptors_engaging_G_alphai_protein_family

description:
  PW:0000856 acetylcholine signaling pathway via muscarinic acetylcholine receptors engaging G alphai protein family


id: 13260
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000353
name:
  Curated.RGD_v4_cfa_gskb_PW:0000353_altered_vascular_endothelial_growth_factor_signaling_pathway_involving_proteins_affecting_its_expression

description:
  PW:0000353 altered vascular endothelial growth factor signaling pathway involving proteins affecting its expression


id: 13262
description: PW:0002139 intermembrane space assembly pathway of mitochondrial protein import
n: 3
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0002139
name:
  Curated.RGD_v4_cfa_gskb_PW:0002139_intermembrane_space_assembly_pathway_of_mitochondrial_protein_import


id: 13303
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000692
name:
  Curated.RGD_v4_cfa_gskb_PW:0000692_altered_insulin_responsive_facilitative_sugar_transporter_mediated_glucose_transport_pathway

description:
  PW:0000692 altered insulin responsive facilitative sugar transporter mediated glucose transport pathway


id: 13314
description: PW:0000341 altered Notch signaling pathway involving the macromolecules modifying the main players
n: 2
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000341
name:
  Curated.RGD_v4_cfa_gskb_PW:0000341_altered_Notch_signaling_pathway_involving_the_macromolecules_modifying_the_main_players


id: 13359
description: PW:0000623 altered scatter factor/hepatocyte growth factor signaling pathway
n: 1
memo: https://rgd.mcw.edu/rgdweb/ontology/annot.html?acc_id=PW:0000623
name:
  Curated.RGD_v4_cfa_gskb_PW:0000623_altered_scatter_factor/hepatocyte_growth_factor_signaling_pathway


id: 13838
description: P00031 Inflammation mediated by chemokine and cytokine signaling pathway
n: 6
memo: https://www.pantherdb.org/pathway/pathDetail.do?clsAccession=P00031
name:
  Curated.PANTHER_v4_cfa_gskb_P00031_Inflammation_mediated_by_chemokine_and_cytokine_signaling_pathway


id: 13845
description: P00026 Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
n: 5
memo: https://www.pantherdb.org/pathway/pathDetail.do?clsAccession=P00026
name:
  Curated.PANTHER_v4_cfa_gskb_P00026_Heterotrimeric_G-protein_signaling_pathway-Gi_alpha_and_Gs_alpha_mediated_pathway


id: 13846
description: P00027 Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway
n: 4
memo: https://www.pantherdb.org/pathway/pathDetail.do?clsAccession=P00027
name:
  Curated.PANTHER_v4_cfa_gskb_P00027_Heterotrimeric_G-protein_signaling_pathway-Gq_alpha_and_Go_alpha_mediated_pathway


id: 13865
description: P05911 Angiotensin II-stimulated signaling through G proteins and beta-arrestin
n: 1
memo: https://www.pantherdb.org/pathway/pathDetail.do?clsAccession=P05911
name:
  Curated.PANTHER_v4_cfa_gskb_P05911_Angiotensin_II-stimulated_signaling_through_G_proteins_and_beta-arrestin


id: 13867
description: P00028 Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction
n: 4
memo: https://www.pantherdb.org/pathway/pathDetail.do?clsAccession=P00028
name:
  Curated.PANTHER_v4_cfa_gskb_P00028_Heterotrimeric_G-protein_signaling_pathway-rod_outer_segment_phototransduction


id: 13894
description: P00032 Insulin/IGF pathway-mitogen activated protein kinase kinase/MAP kinase cascade
n: 1
memo: https://www.pantherdb.org/pathway/pathDetail.do?clsAccession=P00032
name:
  Curated.PANTHER_v4_cfa_gskb_P00032_Insulin/IGF_pathway-mitogen_activated_protein_kinase_kinase/MAP_kinase_cascade


id: 32777
description: GO:0000184 Nuclear-transcribed mrna catabolic process nonsense-mediated decay
n: 31
memo: https://amigo.geneontology.org/amigo/term/GO:0000184
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000184_Nuclear-transcribed_mrna_catabolic_process_nonsense-mediated_decay 


id: 32791
description: GO:0000288 Nuclear-transcribed mrna catabolic process deadenylation-dependent decay
n: 41
memo: https://amigo.geneontology.org/amigo/term/GO:0000288
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000288_Nuclear-transcribed_mrna_catabolic_process_deadenylation-dependent_decay 


id: 32793
description: GO:0000290 Deadenylation-dependent decapping of nuclear-transcribed mrna
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0000290
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000290_Deadenylation-dependent_decapping_of_nuclear-transcribed_mrna 


id: 32800
description: GO:0000350 Generation of catalytic spliceosome for second transesterification step
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0000350
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000350_Generation_of_catalytic_spliceosome_for_second_transesterification_step 


id: 32802
description: GO:0000377 Rna splicing via transesterification reactions with bulged adenosine as nucleophile
n: 263
memo: https://amigo.geneontology.org/amigo/term/GO:0000377
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000377_Rna_splicing_via_transesterification_reactions_with_bulged_adenosine_as_nucleophile 


id: 32807
description: GO:0000393 Spliceosomal conformational changes to generate catalytic conformation
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0000393
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000393_Spliceosomal_conformational_changes_to_generate_catalytic_conformation 


id: 32814
description: GO:0000429 Carbon catabolite regulation of transcription from rna polymerase ii promoter
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0000429
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000429_Carbon_catabolite_regulation_of_transcription_from_rna_polymerase_ii_promoter 


id: 32815
description: GO:0000430 Regulation of transcription from rna polymerase ii promoter by glucose
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0000430
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000430_Regulation_of_transcription_from_rna_polymerase_ii_promoter_by_glucose 


id: 32816
description: GO:0000432 Positive regulation of transcription from rna polymerase ii promoter by glucose
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0000432
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000432_Positive_regulation_of_transcription_from_rna_polymerase_ii_promoter_by_glucose 


id: 32817
description: GO:0000436 Carbon catabolite activation of transcription from rna polymerase ii promoter
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0000436
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000436_Carbon_catabolite_activation_of_transcription_from_rna_polymerase_ii_promoter 


id: 32818
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0000447
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000447_Endonucleolytic_cleavage_in_its1_to_separate_ssu-rrna_from_5.8s_rrna_and_lsu-rrna_from_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 

description:
  GO:0000447 Endonucleolytic cleavage in its1 to separate ssu-rrna from 5.8s rrna and lsu-rrna from tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna) 


id: 32822
description: GO:0000462 Maturation of ssu-rrna from tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna)
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0000462
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000462_Maturation_of_ssu-rrna_from_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 


id: 32823
description: GO:0000463 Maturation of lsu-rrna from tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna)
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0000463
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000463_Maturation_of_lsu-rrna_from_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 


id: 32824
description: GO:0000466 Maturation of 5.8s rrna from tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna)
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0000466
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000466_Maturation_of_5.8s_rrna_from_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 


id: 32825
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0000467
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000467_Exonucleolytic_trimming_to_generate_mature_3-prime-end_of_5.8s_rrna_from_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 

description:
  GO:0000467 Exonucleolytic trimming to generate mature 3-prime-end of 5.8s rrna from tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna) 


id: 32827
description: GO:0000479 Endonucleolytic cleavage of tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna)
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0000479
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000479_Endonucleolytic_cleavage_of_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 


id: 32828
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0000480
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000480_Endonucleolytic_cleavage_in_5-prime-ets_of_tricistronic_rrna_transcript_(ssu-rrna_5.8s_rrna_lsu-rrna) 

description:
  GO:0000480 Endonucleolytic cleavage in 5-prime-ets of tricistronic rrna transcript (ssu-rrna 5.8s rrna lsu-rrna) 


id: 32862
description: GO:0000972 Transcription-dependent tethering of rna polymerase ii gene dna at nuclear periphery
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0000972
name:
  GOBP_clfamiliaris_ens_gskb_GO:0000972_Transcription-dependent_tethering_of_rna_polymerase_ii_gene_dna_at_nuclear_periphery 


id: 32868
description: GO:0001174 Transcriptional start site selection at rna polymerase ii promoter
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0001174
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001174_Transcriptional_start_site_selection_at_rna_polymerase_ii_promoter 


id: 32908
description: GO:0001580 Detection of chemical stimulus involved in sensory perception of bitter taste
n: 18
memo: https://amigo.geneontology.org/amigo/term/GO:0001580
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001580_Detection_of_chemical_stimulus_involved_in_sensory_perception_of_bitter_taste 


id: 32909
description: GO:0001582 Detection of chemical stimulus involved in sensory perception of sweet taste
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0001582
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001582_Detection_of_chemical_stimulus_involved_in_sensory_perception_of_sweet_taste 


id: 33059
description: GO:0001976 Nervous system process involved in regulation of systemic arterial blood pressure
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0001976
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001976_Nervous_system_process_involved_in_regulation_of_systemic_arterial_blood_pressure 


id: 33061
description: GO:0001978 Regulation of systemic arterial blood pressure by carotid sinus baroreceptor feedback
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0001978
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001978_Regulation_of_systemic_arterial_blood_pressure_by_carotid_sinus_baroreceptor_feedback 


id: 33063
description: GO:0001991 Regulation of systemic arterial blood pressure by circulatory renin-angiotensin
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0001991
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001991_Regulation_of_systemic_arterial_blood_pressure_by_circulatory_renin-angiotensin 


id: 33064
description: GO:0001992 Regulation of systemic arterial blood pressure by vasopressin
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0001992
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001992_Regulation_of_systemic_arterial_blood_pressure_by_vasopressin 


id: 33065
description: GO:0001993 Regulation of systemic arterial blood pressure by norepinephrine-epinephrine
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0001993
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001993_Regulation_of_systemic_arterial_blood_pressure_by_norepinephrine-epinephrine 


id: 33066
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0001994
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001994_Norepinephrine-epinephrine_vasoconstriction_involved_in_regulation_of_systemic_arterial_blood_pressure 

description:
  GO:0001994 Norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure 


id: 33067
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0001999
name:
  GOBP_clfamiliaris_ens_gskb_GO:0001999_Renal_response_to_blood_flow_involved_in_circulatory_renin-angiotensin_regulation_of_systemic_arterial_blood_pressure 

description:
  GO:0001999 Renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure 


id: 33077
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002025
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002025_Norepinephrine-epinephrine-mediated_vasodilation_involved_in_regulation_of_systemic_arterial_blood_pressure 

description:
  GO:0002025 Norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure 


id: 33081
description: GO:0002029 Desensitization of g protein-coupled receptor signaling pathway
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0002029
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002029_Desensitization_of_g_protein-coupled_receptor_signaling_pathway 


id: 33083
description: GO:0002034 Maintenance of blood vessel diameter homeostasis by renin-angiotensin
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0002034
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002034_Maintenance_of_blood_vessel_diameter_homeostasis_by_renin-angiotensin 


id: 33085
description: GO:0002038 Positive regulation of l-glutamate import across plasma membrane
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0002038
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002038_Positive_regulation_of_l-glutamate_import_across_plasma_membrane 


id: 33088
description: GO:0002043 Blood vessel endothelial cell proliferation involved in sprouting angiogenesis
n: 18
memo: https://amigo.geneontology.org/amigo/term/GO:0002043
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002043_Blood_vessel_endothelial_cell_proliferation_involved_in_sprouting_angiogenesis 


id: 33102
description: GO:0002072 Optic cup morphogenesis involved in camera-type eye development
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002072
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002072_Optic_cup_morphogenesis_involved_in_camera-type_eye_development 


id: 33106
description: GO:0002087 Regulation of respiratory gaseous exchange by nervous system process
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0002087
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002087_Regulation_of_respiratory_gaseous_exchange_by_nervous_system_process 


id: 33122
description: GO:0002157 Positive regulation of thyroid hormone receptor signaling pathway
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002157
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002157_Positive_regulation_of_thyroid_hormone_receptor_signaling_pathway 


id: 33133
description: GO:0002204 Somatic recombination of immunoglobulin genes involved in immune response
n: 44
memo: https://amigo.geneontology.org/amigo/term/GO:0002204
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002204_Somatic_recombination_of_immunoglobulin_genes_involved_in_immune_response 


id: 33134
description: GO:0002208 Somatic diversification of immunoglobulins involved in immune response
n: 44
memo: https://amigo.geneontology.org/amigo/term/GO:0002208
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002208_Somatic_diversification_of_immunoglobulins_involved_in_immune_response 


id: 33137
description: GO:0002220 Innate immune response activating cell surface receptor signaling pathway
n: 58
memo: https://amigo.geneontology.org/amigo/term/GO:0002220
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002220_Innate_immune_response_activating_cell_surface_receptor_signaling_pathway 


id: 33150
description: GO:0002248 Connective tissue replacement involved in inflammatory response wound healing
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0002248
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002248_Connective_tissue_replacement_involved_in_inflammatory_response_wound_healing 


id: 33168
description: GO:0002277 Myeloid dendritic cell activation involved in immune response
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002277
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002277_Myeloid_dendritic_cell_activation_involved_in_immune_response 


id: 33176
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0002291
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002291_T_cell_activation_via_t_cell_receptor_contact_with_antigen_bound_to_mhc_molecule_on_antigen_presenting_cell 

description:
  GO:0002291 T cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell 


id: 33178
description: GO:0002293 Alpha-beta t cell differentiation involved in immune response
n: 56
memo: https://amigo.geneontology.org/amigo/term/GO:0002293
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002293_Alpha-beta_t_cell_differentiation_involved_in_immune_response 


id: 33179
description: GO:0002294 Cd4-positive alpha-beta t cell differentiation involved in immune response
n: 55
memo: https://amigo.geneontology.org/amigo/term/GO:0002294
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002294_Cd4-positive_alpha-beta_t_cell_differentiation_involved_in_immune_response 


id: 33183
description: GO:0002305 Cd8-positive gamma-delta intraepithelial t cell differentiation
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002305
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002305_Cd8-positive_gamma-delta_intraepithelial_t_cell_differentiation 


id: 33195
description: GO:0002325 Natural killer cell differentiation involved in immune response
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002325
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002325_Natural_killer_cell_differentiation_involved_in_immune_response 


id: 33215
description: GO:0002361 Cd4-positive cd25-positive alpha-beta regulatory t cell differentiation
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0002361
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002361_Cd4-positive_cd25-positive_alpha-beta_regulatory_t_cell_differentiation 


id: 33225
description: GO:0002381 Immunoglobulin production involved in immunoglobulin-mediated immune response
n: 46
memo: https://amigo.geneontology.org/amigo/term/GO:0002381
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002381_Immunoglobulin_production_involved_in_immunoglobulin-mediated_immune_response 


id: 33235
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002415
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002415_Immunoglobulin_transcytosis_in_epithelial_cells_mediated_by_polymeric_immunoglobulin_receptor 

description:
  GO:0002415 Immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor 


id: 33237
description: GO:0002420 Natural killer cell mediated cytotoxicity directed against tumor cell target
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0002420
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002420_Natural_killer_cell_mediated_cytotoxicity_directed_against_tumor_cell_target 


id: 33240
description: GO:0002428 Antigen processing and presentation of peptide antigen via mhc class ib
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0002428
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002428_Antigen_processing_and_presentation_of_peptide_antigen_via_mhc_class_ib 


id: 33241
description: GO:0002429 Immune response-activating cell surface receptor signaling pathway
n: 180
memo: https://amigo.geneontology.org/amigo/term/GO:0002429
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002429_Immune_response-activating_cell_surface_receptor_signaling_pathway 


id: 33244
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002433
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002433_Immune_response-regulating_cell_surface_receptor_signaling_pathway_involved_in_phagocytosis 

description:
  GO:0002433 Immune response-regulating cell surface receptor signaling pathway involved in phagocytosis 


id: 33258
description: GO:0002455 Humoral immune response mediated by circulating immunoglobulin
n: 27
memo: https://amigo.geneontology.org/amigo/term/GO:0002455
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002455_Humoral_immune_response_mediated_by_circulating_immunoglobulin 


id: 33262
n: 200
memo: https://amigo.geneontology.org/amigo/term/GO:0002460
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002460_Adaptive_immune_response_based_on_somatic_recombination_of_immune_receptors_built_from_immunoglobulin_superfamily_domains 

description:
  GO:0002460 Adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains 


id: 33267
description: GO:0002474 Antigen processing and presentation of peptide antigen via mhc class i
n: 16
memo: https://amigo.geneontology.org/amigo/term/GO:0002474
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002474_Antigen_processing_and_presentation_of_peptide_antigen_via_mhc_class_i 


id: 33269
description: GO:0002476 Antigen processing and presentation of endogenous peptide antigen via mhc class ib
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002476
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002476_Antigen_processing_and_presentation_of_endogenous_peptide_antigen_via_mhc_class_ib 


id: 33270
description: GO:0002477 Antigen processing and presentation of exogenous peptide antigen via mhc class ib
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002477
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002477_Antigen_processing_and_presentation_of_exogenous_peptide_antigen_via_mhc_class_ib 


id: 33271
description: GO:0002478 Antigen processing and presentation of exogenous peptide antigen
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0002478
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002478_Antigen_processing_and_presentation_of_exogenous_peptide_antigen 


id: 33272
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002481
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002481_Antigen_processing_and_presentation_of_exogenous_protein_antigen_via_mhc_class_ib_tap-dependent 

description:
  GO:0002481 Antigen processing and presentation of exogenous protein antigen via mhc class ib tap-dependent 


id: 33273
description: GO:0002483 Antigen processing and presentation of endogenous peptide antigen
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0002483
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002483_Antigen_processing_and_presentation_of_endogenous_peptide_antigen 


id: 33274
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002484
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002484_Antigen_processing_and_presentation_of_endogenous_peptide_antigen_via_mhc_class_i_via_er_pathway 

description:
  GO:0002484 Antigen processing and presentation of endogenous peptide antigen via mhc class i via er pathway 


id: 33275
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002486
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002486_Antigen_processing_and_presentation_of_endogenous_peptide_antigen_via_mhc_class_i_via_er_pathway_tap-independent 

description:
  GO:0002486 Antigen processing and presentation of endogenous peptide antigen via mhc class i via er pathway tap-independent 


id: 33276
description: GO:0002495 Antigen processing and presentation of peptide antigen via mhc class ii
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0002495
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002495_Antigen_processing_and_presentation_of_peptide_antigen_via_mhc_class_ii 


id: 33280
n: 18
memo: https://amigo.geneontology.org/amigo/term/GO:0002504
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002504_Antigen_processing_and_presentation_of_peptide_or_polysaccharide_antigen_via_mhc_class_ii 

description:
  GO:0002504 Antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii 


id: 33293
description: GO:0002528 Regulation of vascular permeability involved in acute inflammatory response
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002528
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002528_Regulation_of_vascular_permeability_involved_in_acute_inflammatory_response 


id: 33294
description: GO:0002532 Production of molecular mediator involved in inflammatory response
n: 57
memo: https://amigo.geneontology.org/amigo/term/GO:0002532
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002532_Production_of_molecular_mediator_involved_in_inflammatory_response 


id: 33297
description: GO:0002538 Arachidonate metabolite production involved in inflammatory response
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002538
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002538_Arachidonate_metabolite_production_involved_in_inflammatory_response 


id: 33299
description: GO:0002541 Activation of plasma proteins involved in acute inflammatory response
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002541
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002541_Activation_of_plasma_proteins_involved_in_acute_inflammatory_response 


id: 33305
n: 55
memo: https://amigo.geneontology.org/amigo/term/GO:0002562
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002562_Somatic_diversification_of_immune_receptors_via_germline_recombination_within_a_single_locus 

description:
  GO:0002562 Somatic diversification of immune receptors via germline recombination within a single locus 


id: 33306
description: GO:0002566 Somatic diversification of immune receptors via somatic mutation
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0002566
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002566_Somatic_diversification_of_immune_receptors_via_somatic_mutation 


id: 33314
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002580
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002580_Regulation_of_antigen_processing_and_presentation_of_peptide_or_polysaccharide_antigen_via_mhc_class_ii 

description:
  GO:0002580 Regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii 


id: 33315
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002581
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002581_Negative_regulation_of_antigen_processing_and_presentation_of_peptide_or_polysaccharide_antigen_via_mhc_class_ii 

description:
  GO:0002581 Negative regulation of antigen processing and presentation of peptide or polysaccharide antigen via mhc class ii 


id: 33316
description: GO:0002583 Regulation of antigen processing and presentation of peptide antigen
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0002583
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002583_Regulation_of_antigen_processing_and_presentation_of_peptide_antigen 


id: 33317
description: GO:0002584 Negative regulation of antigen processing and presentation of peptide antigen
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002584
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002584_Negative_regulation_of_antigen_processing_and_presentation_of_peptide_antigen 


id: 33318
description: GO:0002586 Regulation of antigen processing and presentation of peptide antigen via mhc class ii
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002586
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002586_Regulation_of_antigen_processing_and_presentation_of_peptide_antigen_via_mhc_class_ii 


id: 33319
description: GO:0002589 Regulation of antigen processing and presentation of peptide antigen via mhc class i
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002589
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002589_Regulation_of_antigen_processing_and_presentation_of_peptide_antigen_via_mhc_class_i 


id: 33320
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002590
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002590_Negative_regulation_of_antigen_processing_and_presentation_of_peptide_antigen_via_mhc_class_i 

description:
  GO:0002590 Negative regulation of antigen processing and presentation of peptide antigen via mhc class i 


id: 33321
description: GO:0002604 Regulation of dendritic cell antigen processing and presentation
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0002604
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002604_Regulation_of_dendritic_cell_antigen_processing_and_presentation 


id: 33322
description: GO:0002605 Negative regulation of dendritic cell antigen processing and presentation
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002605
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002605_Negative_regulation_of_dendritic_cell_antigen_processing_and_presentation 


id: 33323
description: GO:0002606 Positive regulation of dendritic cell antigen processing and presentation
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0002606
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002606_Positive_regulation_of_dendritic_cell_antigen_processing_and_presentation 


id: 33331
description: GO:0002652 Regulation of tolerance induction dependent upon immune response
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002652
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002652_Regulation_of_tolerance_induction_dependent_upon_immune_response 


id: 33364
description: GO:0002700 Regulation of production of molecular mediator of immune response
n: 127
memo: https://amigo.geneontology.org/amigo/term/GO:0002700
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002700_Regulation_of_production_of_molecular_mediator_of_immune_response 


id: 33365
description: GO:0002701 Negative regulation of production of molecular mediator of immune response
n: 28
memo: https://amigo.geneontology.org/amigo/term/GO:0002701
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002701_Negative_regulation_of_production_of_molecular_mediator_of_immune_response 


id: 33366
description: GO:0002702 Positive regulation of production of molecular mediator of immune response
n: 88
memo: https://amigo.geneontology.org/amigo/term/GO:0002702
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002702_Positive_regulation_of_production_of_molecular_mediator_of_immune_response 


id: 33382
description: GO:0002718 Regulation of cytokine production involved in immune response
n: 79
memo: https://amigo.geneontology.org/amigo/term/GO:0002718
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002718_Regulation_of_cytokine_production_involved_in_immune_response 


id: 33383
description: GO:0002719 Negative regulation of cytokine production involved in immune response
n: 23
memo: https://amigo.geneontology.org/amigo/term/GO:0002719
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002719_Negative_regulation_of_cytokine_production_involved_in_immune_response 


id: 33384
description: GO:0002720 Positive regulation of cytokine production involved in immune response
n: 49
memo: https://amigo.geneontology.org/amigo/term/GO:0002720
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002720_Positive_regulation_of_cytokine_production_involved_in_immune_response 


id: 33389
description: GO:0002729 Positive regulation of natural killer cell cytokine production
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002729
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002729_Positive_regulation_of_natural_killer_cell_cytokine_production 


id: 33393
description: GO:0002735 Positive regulation of myeloid dendritic cell cytokine production
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002735
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002735_Positive_regulation_of_myeloid_dendritic_cell_cytokine_production 


id: 33407
description: GO:0002767 Immune response-inhibiting cell surface receptor signaling pathway
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002767
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002767_Immune_response-inhibiting_cell_surface_receptor_signaling_pathway 


id: 33408
description: GO:0002768 Immune response-regulating cell surface receptor signaling pathway
n: 191
memo: https://amigo.geneontology.org/amigo/term/GO:0002768
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002768_Immune_response-regulating_cell_surface_receptor_signaling_pathway 


id: 33423
n: 126
memo: https://amigo.geneontology.org/amigo/term/GO:0002822
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002822_Regulation_of_adaptive_immune_response_based_on_somatic_recombination_of_immune_receptors_built_from_immunoglobulin_superfamily_domains 

description:
  GO:0002822 Regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains 


id: 33424
n: 38
memo: https://amigo.geneontology.org/amigo/term/GO:0002823
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002823_Negative_regulation_of_adaptive_immune_response_based_on_somatic_recombination_of_immune_receptors_built_from_immunoglobulin_superfamily_domains 

description:
  GO:0002823 Negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains 


id: 33425
n: 83
memo: https://amigo.geneontology.org/amigo/term/GO:0002824
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002824_Positive_regulation_of_adaptive_immune_response_based_on_somatic_recombination_of_immune_receptors_built_from_immunoglobulin_superfamily_domains 

description:
  GO:0002824 Positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains 


id: 33442
description: GO:0002841 Negative regulation of t cell mediated immune response to tumor cell
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002841
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002841_Negative_regulation_of_t_cell_mediated_immune_response_to_tumor_cell 


id: 33443
description: GO:0002842 Positive regulation of t cell mediated immune response to tumor cell
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0002842
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002842_Positive_regulation_of_t_cell_mediated_immune_response_to_tumor_cell 


id: 33444
description: GO:0002855 Regulation of natural killer cell mediated immune response to tumor cell
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0002855
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002855_Regulation_of_natural_killer_cell_mediated_immune_response_to_tumor_cell 


id: 33445
description: GO:0002856 Negative regulation of natural killer cell mediated immune response to tumor cell
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002856
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002856_Negative_regulation_of_natural_killer_cell_mediated_immune_response_to_tumor_cell 


id: 33446
description: GO:0002857 Positive regulation of natural killer cell mediated immune response to tumor cell
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0002857
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002857_Positive_regulation_of_natural_killer_cell_mediated_immune_response_to_tumor_cell 


id: 33447
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0002858
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002858_Regulation_of_natural_killer_cell_mediated_cytotoxicity_directed_against_tumor_cell_target 

description:
  GO:0002858 Regulation of natural killer cell mediated cytotoxicity directed against tumor cell target 


id: 33448
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002859
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002859_Negative_regulation_of_natural_killer_cell_mediated_cytotoxicity_directed_against_tumor_cell_target 

description:
  GO:0002859 Negative regulation of natural killer cell mediated cytotoxicity directed against tumor cell target 


id: 33449
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0002860
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002860_Positive_regulation_of_natural_killer_cell_mediated_cytotoxicity_directed_against_tumor_cell_target 

description:
  GO:0002860 Positive regulation of natural killer cell mediated cytotoxicity directed against tumor cell target 


id: 33451
description: GO:0002862 Negative regulation of inflammatory response to antigenic stimulus
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0002862
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002862_Negative_regulation_of_inflammatory_response_to_antigenic_stimulus 


id: 33452
description: GO:0002863 Positive regulation of inflammatory response to antigenic stimulus
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0002863
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002863_Positive_regulation_of_inflammatory_response_to_antigenic_stimulus 


id: 33453
description: GO:0002864 Regulation of acute inflammatory response to antigenic stimulus
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0002864
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002864_Regulation_of_acute_inflammatory_response_to_antigenic_stimulus 


id: 33454
description: GO:0002865 Negative regulation of acute inflammatory response to antigenic stimulus
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002865
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002865_Negative_regulation_of_acute_inflammatory_response_to_antigenic_stimulus 


id: 33455
description: GO:0002866 Positive regulation of acute inflammatory response to antigenic stimulus
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002866
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002866_Positive_regulation_of_acute_inflammatory_response_to_antigenic_stimulus 


id: 33457
description: GO:0002874 Regulation of chronic inflammatory response to antigenic stimulus
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0002874
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002874_Regulation_of_chronic_inflammatory_response_to_antigenic_stimulus 


id: 33458
description: GO:0002876 Positive regulation of chronic inflammatory response to antigenic stimulus
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002876
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002876_Positive_regulation_of_chronic_inflammatory_response_to_antigenic_stimulus 


id: 33459
description: GO:0002877 Regulation of acute inflammatory response to non-antigenic stimulus
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002877
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002877_Regulation_of_acute_inflammatory_response_to_non-antigenic_stimulus 


id: 33460
description: GO:0002879 Positive regulation of acute inflammatory response to non-antigenic stimulus
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0002879
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002879_Positive_regulation_of_acute_inflammatory_response_to_non-antigenic_stimulus 


id: 33467
description: GO:0002890 Negative regulation of immunoglobulin mediated immune response
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0002890
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002890_Negative_regulation_of_immunoglobulin_mediated_immune_response 


id: 33468
description: GO:0002891 Positive regulation of immunoglobulin mediated immune response
n: 32
memo: https://amigo.geneontology.org/amigo/term/GO:0002891
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002891_Positive_regulation_of_immunoglobulin_mediated_immune_response 


id: 33480
description: GO:0002923 Regulation of humoral immune response mediated by circulating immunoglobulin
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0002923
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002923_Regulation_of_humoral_immune_response_mediated_by_circulating_immunoglobulin 


id: 33481
description: GO:0002924 Negative regulation of humoral immune response mediated by circulating immunoglobulin
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0002924
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002924_Negative_regulation_of_humoral_immune_response_mediated_by_circulating_immunoglobulin 


id: 33482
description: GO:0002925 Positive regulation of humoral immune response mediated by circulating immunoglobulin
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0002925
name:
  GOBP_clfamiliaris_ens_gskb_GO:0002925_Positive_regulation_of_humoral_immune_response_mediated_by_circulating_immunoglobulin 


id: 33504
description: GO:0003025 Regulation of systemic arterial blood pressure by baroreceptor feedback
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0003025
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003025_Regulation_of_systemic_arterial_blood_pressure_by_baroreceptor_feedback 


id: 33505
description: GO:0003044 Regulation of systemic arterial blood pressure mediated by a chemical signal
n: 31
memo: https://amigo.geneontology.org/amigo/term/GO:0003044
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003044_Regulation_of_systemic_arterial_blood_pressure_mediated_by_a_chemical_signal 


id: 33506
description: GO:0003050 Regulation of systemic arterial blood pressure by atrial natriuretic peptide
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0003050
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003050_Regulation_of_systemic_arterial_blood_pressure_by_atrial_natriuretic_peptide 


id: 33508
description: GO:0003057 Regulation of the force of heart contraction by chemical signal
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0003057
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003057_Regulation_of_the_force_of_heart_contraction_by_chemical_signal 


id: 33510
description: GO:0003071 Renal system process involved in regulation of systemic arterial blood pressure
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0003071
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003071_Renal_system_process_involved_in_regulation_of_systemic_arterial_blood_pressure 


id: 33511
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0003072
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003072_Renal_control_of_peripheral_vascular_resistance_involved_in_regulation_of_systemic_arterial_blood_pressure 

description:
  GO:0003072 Renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure 


id: 33513
description: GO:0003081 Regulation of systemic arterial blood pressure by renin-angiotensin
n: 17
memo: https://amigo.geneontology.org/amigo/term/GO:0003081
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003081_Regulation_of_systemic_arterial_blood_pressure_by_renin-angiotensin 


id: 33563
description: GO:0003198 Epithelial to mesenchymal transition involved in endocardial cushion formation
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0003198
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003198_Epithelial_to_mesenchymal_transition_involved_in_endocardial_cushion_formation 


id: 33564
description: GO:0003199 Endocardial cushion to mesenchymal transition involved in heart valve formation
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0003199
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003199_Endocardial_cushion_to_mesenchymal_transition_involved_in_heart_valve_formation 


id: 33588
description: GO:0003250 Regulation of cell proliferation involved in heart valve morphogenesis
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0003250
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003250_Regulation_of_cell_proliferation_involved_in_heart_valve_morphogenesis 


id: 33589
description: GO:0003252 Negative regulation of cell proliferation involved in heart valve morphogenesis
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0003252
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003252_Negative_regulation_of_cell_proliferation_involved_in_heart_valve_morphogenesis 


id: 33590
description: GO:0003253 Cardiac neural crest cell migration involved in outflow tract morphogenesis
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0003253
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003253_Cardiac_neural_crest_cell_migration_involved_in_outflow_tract_morphogenesis 


id: 33594
description: GO:0003266 Regulation of secondary heart field cardioblast proliferation
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0003266
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003266_Regulation_of_secondary_heart_field_cardioblast_proliferation 


id: 33614
description: GO:0003321 Positive regulation of blood pressure by epinephrine-norepinephrine
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0003321
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003321_Positive_regulation_of_blood_pressure_by_epinephrine-norepinephrine 


id: 33617
description: GO:0003331 Positive regulation of extracellular matrix constituent secretion
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0003331
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003331_Positive_regulation_of_extracellular_matrix_constituent_secretion 


id: 33618
description: GO:0003332 Negative regulation of extracellular matrix constituent secretion
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0003332
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003332_Negative_regulation_of_extracellular_matrix_constituent_secretion 


id: 33622
description: GO:0003337 Mesenchymal to epithelial transition involved in metanephros morphogenesis
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0003337
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003337_Mesenchymal_to_epithelial_transition_involved_in_metanephros_morphogenesis 


id: 33624
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0003339
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003339_Regulation_of_mesenchymal_to_epithelial_transition_involved_in_metanephros_morphogenesis 

description:
  GO:0003339 Regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis 


id: 33628
description: GO:0003351 Epithelial cilium movement involved in extracellular fluid movement
n: 30
memo: https://amigo.geneontology.org/amigo/term/GO:0003351
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003351_Epithelial_cilium_movement_involved_in_extracellular_fluid_movement 


id: 33643
description: GO:0003413 Chondrocyte differentiation involved in endochondral bone morphogenesis
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0003413
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003413_Chondrocyte_differentiation_involved_in_endochondral_bone_morphogenesis 


id: 33652
description: GO:0003433 Chondrocyte development involved in endochondral bone morphogenesis
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0003433
name:
  GOBP_clfamiliaris_ens_gskb_GO:0003433_Chondrocyte_development_involved_in_endochondral_bone_morphogenesis 


id: 33845
description: GO:0006398 Mrna 3-prime-end processing by stem-loop binding and cleavage
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0006398
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006398_Mrna_3-prime-end_processing_by_stem-loop_binding_and_cleavage 


id: 33902
description: GO:0006515 Protein quality control for misfolded or incompletely synthesized proteins
n: 20
memo: https://amigo.geneontology.org/amigo/term/GO:0006515
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006515_Protein_quality_control_for_misfolded_or_incompletely_synthesized_proteins 


id: 33979
description: GO:0006616 Srp-dependent cotranslational protein targeting to membrane translocation
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0006616
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006616_Srp-dependent_cotranslational_protein_targeting_to_membrane_translocation 


id: 33980
description: GO:0006617 Srp-dependent cotranslational protein targeting to membrane signal sequence recognition
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0006617
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006617_Srp-dependent_cotranslational_protein_targeting_to_membrane_signal_sequence_recognition 


id: 33981
description: GO:0006620 Post-translational protein targeting to endoplasmic reticulum membrane
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0006620
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006620_Post-translational_protein_targeting_to_endoplasmic_reticulum_membrane 


id: 33987
description: GO:0006627 Protein processing involved in protein targeting to mitochondrion
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0006627
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006627_Protein_processing_involved_in_protein_targeting_to_mitochondrion 


id: 34133
description: GO:0006890 Retrograde vesicle-mediated transport golgi to endoplasmic reticulum
n: 33
memo: https://amigo.geneontology.org/amigo/term/GO:0006890
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006890_Retrograde_vesicle-mediated_transport_golgi_to_endoplasmic_reticulum 


id: 34153
description: GO:0006921 Cellular component disassembly involved in execution phase of apoptosis
n: 20
memo: https://amigo.geneontology.org/amigo/term/GO:0006921
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006921_Cellular_component_disassembly_involved_in_execution_phase_of_apoptosis 


id: 34158
description: GO:0006931 Substrate-dependent cell migration cell attachment to substrate
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0006931
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006931_Substrate-dependent_cell_migration_cell_attachment_to_substrate 


id: 34159
description: GO:0006933 Negative regulation of cell adhesion involved in substrate-bound cell migration
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0006933
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006933_Negative_regulation_of_cell_adhesion_involved_in_substrate-bound_cell_migration 


id: 34182
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0006977
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006977_Dna_damage_response_signal_transduction_by_p53_class_mediator_resulting_in_cell_cycle_arrest 

description:
  GO:0006977 Dna damage response signal transduction by p53 class mediator resulting in cell cycle arrest 


id: 34183
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0006978
name:
  GOBP_clfamiliaris_ens_gskb_GO:0006978_Dna_damage_response_signal_transduction_by_p53_class_mediator_resulting_in_transcription_of_p21_class_mediator 

description:
  GO:0006978 Dna damage response signal transduction by p53 class mediator resulting in transcription of p21 class mediator 


id: 34261
description: GO:0007156 Homophilic cell adhesion via plasma membrane adhesion molecules
n: 91
memo: https://amigo.geneontology.org/amigo/term/GO:0007156
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007156_Homophilic_cell_adhesion_via_plasma_membrane_adhesion_molecules 


id: 34262
description: GO:0007157 Heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
n: 21
memo: https://amigo.geneontology.org/amigo/term/GO:0007157
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007157_Heterophilic_cell-cell_adhesion_via_plasma_membrane_cell_adhesion_molecules 


id: 34274
description: GO:0007169 Cell surface receptor protein tyrosine kinase signaling pathway
n: 434
memo: https://amigo.geneontology.org/amigo/term/GO:0007169
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007169_Cell_surface_receptor_protein_tyrosine_kinase_signaling_pathway 


id: 34277
description: GO:0007175 Negative regulation of epidermal growth factor-activated receptor activity
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0007175
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007175_Negative_regulation_of_epidermal_growth_factor-activated_receptor_activity 


id: 34278
description: GO:0007176 Regulation of epidermal growth factor-activated receptor activity
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0007176
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007176_Regulation_of_epidermal_growth_factor-activated_receptor_activity 


id: 34279
description: GO:0007178 Cell surface receptor protein serine/threonine kinase signaling pathway
n: 265
memo: https://amigo.geneontology.org/amigo/term/GO:0007178
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007178_Cell_surface_receptor_protein_serine/threonine_kinase_signaling_pathway 


id: 34282
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0007187
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007187_G_protein-coupled_receptor_signaling_pathway_coupled_to_cyclic_nucleotide_second_messenger 

description:
  GO:0007187 G protein-coupled receptor signaling pathway coupled to cyclic nucleotide second messenger 


id: 34283
description: GO:0007188 Adenylate cyclase-modulating g protein-coupled receptor signaling pathway
n: 147
memo: https://amigo.geneontology.org/amigo/term/GO:0007188
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007188_Adenylate_cyclase-modulating_g_protein-coupled_receptor_signaling_pathway 


id: 34284
description: GO:0007189 Adenylate cyclase-activating g protein-coupled receptor signaling pathway
n: 95
memo: https://amigo.geneontology.org/amigo/term/GO:0007189
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007189_Adenylate_cyclase-activating_g_protein-coupled_receptor_signaling_pathway 


id: 34285
description: GO:0007191 Adenylate cyclase-activating dopamine receptor signaling pathway
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0007191
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007191_Adenylate_cyclase-activating_dopamine_receptor_signaling_pathway 


id: 34286
description: GO:0007192 Adenylate cyclase-activating serotonin receptor signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0007192
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007192_Adenylate_cyclase-activating_serotonin_receptor_signaling_pathway 


id: 34287
description: GO:0007193 Adenylate cyclase-inhibiting g protein-coupled receptor signaling pathway
n: 52
memo: https://amigo.geneontology.org/amigo/term/GO:0007193
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007193_Adenylate_cyclase-inhibiting_g_protein-coupled_receptor_signaling_pathway 


id: 34288
description: GO:0007195 Adenylate cyclase-inhibiting dopamine receptor signaling pathway
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0007195
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007195_Adenylate_cyclase-inhibiting_dopamine_receptor_signaling_pathway 


id: 34289
description: GO:0007196 Adenylate cyclase-inhibiting g protein-coupled glutamate receptor signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0007196
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007196_Adenylate_cyclase-inhibiting_g_protein-coupled_glutamate_receptor_signaling_pathway 


id: 34290
description: GO:0007197 Adenylate cyclase-inhibiting g protein-coupled acetylcholine receptor signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0007197
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007197_Adenylate_cyclase-inhibiting_g_protein-coupled_acetylcholine_receptor_signaling_pathway 


id: 34291
description: GO:0007198 Adenylate cyclase-inhibiting serotonin receptor signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0007198
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007198_Adenylate_cyclase-inhibiting_serotonin_receptor_signaling_pathway 


id: 34292
description: GO:0007200 Phospholipase c-activating g protein-coupled receptor signaling pathway
n: 66
memo: https://amigo.geneontology.org/amigo/term/GO:0007200
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007200_Phospholipase_c-activating_g_protein-coupled_receptor_signaling_pathway 


id: 34294
description: GO:0007206 Phospholipase c-activating g protein-coupled glutamate receptor signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0007206
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007206_Phospholipase_c-activating_g_protein-coupled_glutamate_receptor_signaling_pathway 


id: 34295
description: GO:0007207 Phospholipase c-activating g protein-coupled acetylcholine receptor signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0007207
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007207_Phospholipase_c-activating_g_protein-coupled_acetylcholine_receptor_signaling_pathway 


id: 34296
description: GO:0007208 Phospholipase c-activating serotonin receptor signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0007208
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007208_Phospholipase_c-activating_serotonin_receptor_signaling_pathway 


id: 34307
description: GO:0007221 Positive regulation of transcription of notch receptor target
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0007221
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007221_Positive_regulation_of_transcription_of_notch_receptor_target 


id: 34343
description: GO:0007342 Fusion of sperm to egg plasma membrane involved in single fertilization
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0007342
name:
  GOBP_clfamiliaris_ens_gskb_GO:0007342_Fusion_of_sperm_to_egg_plasma_membrane_involved_in_single_fertilization 


id: 34506
description: GO:0008625 Extrinsic apoptotic signaling pathway via death domain receptors
n: 61
memo: https://amigo.geneontology.org/amigo/term/GO:0008625
name:
  GOBP_clfamiliaris_ens_gskb_GO:0008625_Extrinsic_apoptotic_signaling_pathway_via_death_domain_receptors 


id: 34507
description: GO:0008627 Intrinsic apoptotic signaling pathway in response to osmotic stress
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0008627
name:
  GOBP_clfamiliaris_ens_gskb_GO:0008627_Intrinsic_apoptotic_signaling_pathway_in_response_to_osmotic_stress 


id: 34508
description: GO:0008630 Intrinsic apoptotic signaling pathway in response to dna damage
n: 70
memo: https://amigo.geneontology.org/amigo/term/GO:0008630
name:
  GOBP_clfamiliaris_ens_gskb_GO:0008630_Intrinsic_apoptotic_signaling_pathway_in_response_to_dna_damage 


id: 34509
description: GO:0008631 Intrinsic apoptotic signaling pathway in response to oxidative stress
n: 39
memo: https://amigo.geneontology.org/amigo/term/GO:0008631
name:
  GOBP_clfamiliaris_ens_gskb_GO:0008631_Intrinsic_apoptotic_signaling_pathway_in_response_to_oxidative_stress 


id: 34545
description: GO:0009095 Aromatic amino acid family biosynthetic process prephenate pathway
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0009095
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009095_Aromatic_amino_acid_family_biosynthetic_process_prephenate_pathway 


id: 34604
description: GO:0009171 Purine deoxyribonucleoside monophosphate biosynthetic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0009171
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009171_Purine_deoxyribonucleoside_monophosphate_biosynthetic_process 


id: 34609
description: GO:0009176 Pyrimidine deoxyribonucleoside monophosphate metabolic process
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0009176
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009176_Pyrimidine_deoxyribonucleoside_monophosphate_metabolic_process 


id: 34610
description: GO:0009177 Pyrimidine deoxyribonucleoside monophosphate biosynthetic process
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0009177
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009177_Pyrimidine_deoxyribonucleoside_monophosphate_biosynthetic_process 


id: 34611
description: GO:0009178 Pyrimidine deoxyribonucleoside monophosphate catabolic process
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0009178
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009178_Pyrimidine_deoxyribonucleoside_monophosphate_catabolic_process 


id: 34633
description: GO:0009211 Pyrimidine deoxyribonucleoside triphosphate metabolic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0009211
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009211_Pyrimidine_deoxyribonucleoside_triphosphate_metabolic_process 


id: 34634
description: GO:0009213 Pyrimidine deoxyribonucleoside triphosphate catabolic process
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0009213
name:
  GOBP_clfamiliaris_ens_gskb_GO:0009213_Pyrimidine_deoxyribonucleoside_triphosphate_catabolic_process 


id: 34812
description: GO:0010248 Establishment or maintenance of transmembrane electrochemical gradient
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0010248
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010248_Establishment_or_maintenance_of_transmembrane_electrochemical_gradient 


id: 34853
description: GO:0010513 Positive regulation of phosphatidylinositol biosynthetic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0010513
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010513_Positive_regulation_of_phosphatidylinositol_biosynthetic_process 


id: 34871
description: GO:0010569 Regulation of double-strand break repair via homologous recombination
n: 61
memo: https://amigo.geneontology.org/amigo/term/GO:0010569
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010569_Regulation_of_double-strand_break_repair_via_homologous_recombination 


id: 34876
description: GO:0010575 Positive regulation of vascular endothelial growth factor production
n: 23
memo: https://amigo.geneontology.org/amigo/term/GO:0010575
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010575_Positive_regulation_of_vascular_endothelial_growth_factor_production 


id: 34888
description: GO:0010606 Positive regulation of cytoplasmic mrna processing body assembly
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0010606
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010606_Positive_regulation_of_cytoplasmic_mrna_processing_body_assembly 


id: 34890
description: GO:0010609 Mrna localization resulting in post-transcriptional regulation of gene expression
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0010609
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010609_Mrna_localization_resulting_in_post-transcriptional_regulation_of_gene_expression 


id: 34911
description: GO:0010640 Regulation of platelet-derived growth factor receptor signaling pathway
n: 18
memo: https://amigo.geneontology.org/amigo/term/GO:0010640
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010640_Regulation_of_platelet-derived_growth_factor_receptor_signaling_pathway 


id: 34912
description: GO:0010641 Positive regulation of platelet-derived growth factor receptor signaling pathway
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0010641
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010641_Positive_regulation_of_platelet-derived_growth_factor_receptor_signaling_pathway 


id: 34913
description: GO:0010642 Negative regulation of platelet-derived growth factor receptor signaling pathway
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0010642
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010642_Negative_regulation_of_platelet-derived_growth_factor_receptor_signaling_pathway 


id: 34926
description: GO:0010663 Positive regulation of striated muscle cell apoptotic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0010663
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010663_Positive_regulation_of_striated_muscle_cell_apoptotic_process 


id: 34927
description: GO:0010664 Negative regulation of striated muscle cell apoptotic process
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0010664
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010664_Negative_regulation_of_striated_muscle_cell_apoptotic_process 


id: 34933
description: GO:0010705 Meiotic dna double-strand break processing involved in reciprocal meiotic recombination
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0010705
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010705_Meiotic_dna_double-strand_break_processing_involved_in_reciprocal_meiotic_recombination 


id: 34950
description: GO:0010729 Positive regulation of hydrogen peroxide biosynthetic process
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0010729
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010729_Positive_regulation_of_hydrogen_peroxide_biosynthetic_process 


id: 34956
description: GO:0010744 Positive regulation of macrophage derived foam cell differentiation
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0010744
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010744_Positive_regulation_of_macrophage_derived_foam_cell_differentiation 


id: 34957
description: GO:0010745 Negative regulation of macrophage derived foam cell differentiation
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0010745
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010745_Negative_regulation_of_macrophage_derived_foam_cell_differentiation 


id: 34958
description: GO:0010746 Regulation of long-chain fatty acid import across plasma membrane
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010746
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010746_Regulation_of_long-chain_fatty_acid_import_across_plasma_membrane 


id: 34959
description: GO:0010748 Negative regulation of long-chain fatty acid import across plasma membrane
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010748
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010748_Negative_regulation_of_long-chain_fatty_acid_import_across_plasma_membrane 


id: 34961
description: GO:0010750 Positive regulation of nitric oxide mediated signal transduction
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0010750
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010750_Positive_regulation_of_nitric_oxide_mediated_signal_transduction 


id: 34962
description: GO:0010751 Negative regulation of nitric oxide mediated signal transduction
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0010751
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010751_Negative_regulation_of_nitric_oxide_mediated_signal_transduction 


id: 34978
description: GO:0010792 Dna double-strand break processing involved in repair via single-strand annealing
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010792
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010792_Dna_double-strand_break_processing_involved_in_repair_via_single-strand_annealing 


id: 34985
description: GO:0010803 Regulation of tumor necrosis factor-mediated signaling pathway
n: 33
memo: https://amigo.geneontology.org/amigo/term/GO:0010803
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010803_Regulation_of_tumor_necrosis_factor-mediated_signaling_pathway 


id: 34986
description: GO:0010804 Negative regulation of tumor necrosis factor-mediated signaling pathway
n: 19
memo: https://amigo.geneontology.org/amigo/term/GO:0010804
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010804_Negative_regulation_of_tumor_necrosis_factor-mediated_signaling_pathway 


id: 35021
description: GO:0010880 Regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0010880
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010880_Regulation_of_release_of_sequestered_calcium_ion_into_cytosol_by_sarcoplasmic_reticulum 


id: 35022
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0010881
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010881_Regulation_of_cardiac_muscle_contraction_by_regulation_of_the_release_of_sequestered_calcium_ion 

description:
  GO:0010881 Regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion 


id: 35023
description: GO:0010882 Regulation of cardiac muscle contraction by calcium ion signaling
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0010882
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010882_Regulation_of_cardiac_muscle_contraction_by_calcium_ion_signaling 


id: 35039
description: GO:0010901 Regulation of very-low-density lipoprotein particle remodeling
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0010901
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010901_Regulation_of_very-low-density_lipoprotein_particle_remodeling 


id: 35040
description: GO:0010903 Negative regulation of very-low-density lipoprotein particle remodeling
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010903
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010903_Negative_regulation_of_very-low-density_lipoprotein_particle_remodeling 


id: 35043
description: GO:0010908 Regulation of heparan sulfate proteoglycan biosynthetic process
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010908
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010908_Regulation_of_heparan_sulfate_proteoglycan_biosynthetic_process 


id: 35044
description: GO:0010909 Positive regulation of heparan sulfate proteoglycan biosynthetic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0010909
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010909_Positive_regulation_of_heparan_sulfate_proteoglycan_biosynthetic_process 


id: 35045
description: GO:0010915 Regulation of very-low-density lipoprotein particle clearance
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010915
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010915_Regulation_of_very-low-density_lipoprotein_particle_clearance 


id: 35046
description: GO:0010916 Negative regulation of very-low-density lipoprotein particle clearance
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010916
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010916_Negative_regulation_of_very-low-density_lipoprotein_particle_clearance 


id: 35054
description: GO:0010944 Negative regulation of transcription by competitive promoter binding
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0010944
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010944_Negative_regulation_of_transcription_by_competitive_promoter_binding 


id: 35078
description: GO:0010989 Negative regulation of low-density lipoprotein particle clearance
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0010989
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010989_Negative_regulation_of_low-density_lipoprotein_particle_clearance 


id: 35082
description: GO:0010998 Regulation of translational initiation by eif2 alpha phosphorylation
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0010998
name:
  GOBP_clfamiliaris_ens_gskb_GO:0010998_Regulation_of_translational_initiation_by_eif2_alpha_phosphorylation 


id: 35120
description: GO:0014717 Regulation of satellite cell activation involved in skeletal muscle regeneration
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0014717
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014717_Regulation_of_satellite_cell_activation_involved_in_skeletal_muscle_regeneration 


id: 35121
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0014718
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014718_Positive_regulation_of_satellite_cell_activation_involved_in_skeletal_muscle_regeneration 

description:
  GO:0014718 Positive regulation of satellite cell activation involved in skeletal muscle regeneration 


id: 35124
description: GO:0014722 Regulation of skeletal muscle contraction by calcium ion signaling
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0014722
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014722_Regulation_of_skeletal_muscle_contraction_by_calcium_ion_signaling 


id: 35137
description: GO:0014808 Release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0014808
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014808_Release_of_sequestered_calcium_ion_into_cytosol_by_sarcoplasmic_reticulum 


id: 35150
description: GO:0014834 Skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0014834
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014834_Skeletal_muscle_satellite_cell_maintenance_involved_in_skeletal_muscle_regeneration 


id: 35164
description: GO:0014862 Regulation of skeletal muscle contraction by chemo-mechanical energy conversion
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0014862
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014862_Regulation_of_skeletal_muscle_contraction_by_chemo-mechanical_energy_conversion 


id: 35167
description: GO:0014873 Response to muscle activity involved in regulation of muscle adaptation
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0014873
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014873_Response_to_muscle_activity_involved_in_regulation_of_muscle_adaptation 


id: 35168
description: GO:0014874 Response to stimulus involved in regulation of muscle adaptation
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0014874
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014874_Response_to_stimulus_involved_in_regulation_of_muscle_adaptation 


id: 35169
description: GO:0014877 Response to muscle inactivity involved in regulation of muscle adaptation
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0014877
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014877_Response_to_muscle_inactivity_involved_in_regulation_of_muscle_adaptation 


id: 35175
description: GO:0014894 Response to denervation involved in regulation of muscle adaptation
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0014894
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014894_Response_to_denervation_involved_in_regulation_of_muscle_adaptation 


id: 35179
description: GO:0014901 Satellite cell activation involved in skeletal muscle regeneration
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0014901
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014901_Satellite_cell_activation_involved_in_skeletal_muscle_regeneration 


id: 35183
description: GO:0014908 Myotube differentiation involved in skeletal muscle regeneration
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0014908
name:
  GOBP_clfamiliaris_ens_gskb_GO:0014908_Myotube_differentiation_involved_in_skeletal_muscle_regeneration 


id: 35190
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0015014
name:
  GOBP_clfamiliaris_ens_gskb_GO:0015014_Heparan_sulfate_proteoglycan_biosynthetic_process_polysaccharide_chain_biosynthetic_process 

description:
  GO:0015014 Heparan sulfate proteoglycan biosynthetic process polysaccharide chain biosynthetic process 


id: 35191
description: GO:0015015 Heparan sulfate proteoglycan biosynthetic process enzymatic modification
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0015015
name:
  GOBP_clfamiliaris_ens_gskb_GO:0015015_Heparan_sulfate_proteoglycan_biosynthetic_process_enzymatic_modification 


id: 35363
description: GO:0016185 Synaptic vesicle budding from presynaptic endocytic zone membrane
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0016185
name:
  GOBP_clfamiliaris_ens_gskb_GO:0016185_Synaptic_vesicle_budding_from_presynaptic_endocytic_zone_membrane 


id: 35391
description: GO:0016338 Calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0016338
name:
  GOBP_clfamiliaris_ens_gskb_GO:0016338_Calcium-independent_cell-cell_adhesion_via_plasma_membrane_cell-adhesion_molecules 


id: 35392
description: GO:0016339 Calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0016339
name:
  GOBP_clfamiliaris_ens_gskb_GO:0016339_Calcium-dependent_cell-cell_adhesion_via_plasma_membrane_cell_adhesion_molecules 


id: 35425
description: GO:0017015 Regulation of transforming growth factor beta receptor signaling pathway
n: 100
memo: https://amigo.geneontology.org/amigo/term/GO:0017015
name:
  GOBP_clfamiliaris_ens_gskb_GO:0017015_Regulation_of_transforming_growth_factor_beta_receptor_signaling_pathway 


id: 35427
description: GO:0017055 Negative regulation of rna polymerase ii transcription preinitiation complex assembly
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0017055
name:
  GOBP_clfamiliaris_ens_gskb_GO:0017055_Negative_regulation_of_rna_polymerase_ii_transcription_preinitiation_complex_assembly 


id: 35477
description: GO:0019219 Regulation of nucleobase-containing compound metabolic process
n: 2696
memo: https://amigo.geneontology.org/amigo/term/GO:0019219
name:
  GOBP_clfamiliaris_ens_gskb_GO:0019219_Regulation_of_nucleobase-containing_compound_metabolic_process 


id: 35489
description: GO:0019243 Methylglyoxal catabolic process to d-lactate via s-lactoyl-glutathione
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0019243
name:
  GOBP_clfamiliaris_ens_gskb_GO:0019243_Methylglyoxal_catabolic_process_to_d-lactate_via_s-lactoyl-glutathione 


id: 35496
description: GO:0019287 Isopentenyl diphosphate biosynthetic process mevalonate pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0019287
name:
  GOBP_clfamiliaris_ens_gskb_GO:0019287_Isopentenyl_diphosphate_biosynthetic_process_mevalonate_pathway 


id: 35589
description: GO:0019885 Antigen processing and presentation of endogenous peptide antigen via mhc class i
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0019885
name:
  GOBP_clfamiliaris_ens_gskb_GO:0019885_Antigen_processing_and_presentation_of_endogenous_peptide_antigen_via_mhc_class_i 


id: 35590
description: GO:0019886 Antigen processing and presentation of exogenous peptide antigen via mhc class ii
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0019886
name:
  GOBP_clfamiliaris_ens_gskb_GO:0019886_Antigen_processing_and_presentation_of_exogenous_peptide_antigen_via_mhc_class_ii 


id: 35702
description: GO:0021775 Smoothened signaling pathway involved in ventral spinal cord interneuron specification
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0021775
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021775_Smoothened_signaling_pathway_involved_in_ventral_spinal_cord_interneuron_specification 


id: 35703
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0021776
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021776_Smoothened_signaling_pathway_involved_in_spinal_cord_motor_neuron_cell_fate_specification 

description:
  GO:0021776 Smoothened signaling pathway involved in spinal cord motor neuron cell fate specification 


id: 35720
description: GO:0021814 Cell motility involved in cerebral cortex radial glia guided migration
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0021814
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021814_Cell_motility_involved_in_cerebral_cortex_radial_glia_guided_migration 


id: 35721
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0021815
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021815_Modulation_of_microtubule_cytoskeleton_involved_in_cerebral_cortex_radial_glia_guided_migration 

description:
  GO:0021815 Modulation of microtubule cytoskeleton involved in cerebral cortex radial glia guided migration 


id: 35722
description: GO:0021817 Nucleokinesis involved in cell motility in cerebral cortex radial glia guided migration
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0021817
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021817_Nucleokinesis_involved_in_cell_motility_in_cerebral_cortex_radial_glia_guided_migration 


id: 35724
description: GO:0021823 Cerebral cortex tangential migration using cell-cell interactions
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0021823
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021823_Cerebral_cortex_tangential_migration_using_cell-cell_interactions 


id: 35728
description: GO:0021828 Gonadotrophin-releasing hormone neuronal migration to the hypothalamus
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0021828
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021828_Gonadotrophin-releasing_hormone_neuronal_migration_to_the_hypothalamus 


id: 35730
description: GO:0021836 Chemorepulsion involved in postnatal olfactory bulb interneuron migration
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0021836
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021836_Chemorepulsion_involved_in_postnatal_olfactory_bulb_interneuron_migration 


id: 35731
description: GO:0021843 Substrate-independent telencephalic tangential interneuron migration
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0021843
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021843_Substrate-independent_telencephalic_tangential_interneuron_migration 


id: 35739
description: GO:0021856 Hypothalamic tangential migration using cell-axon interactions
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0021856
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021856_Hypothalamic_tangential_migration_using_cell-axon_interactions 


id: 35752
description: GO:0021886 Hypothalamus gonadotrophin-releasing hormone neuron differentiation
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0021886
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021886_Hypothalamus_gonadotrophin-releasing_hormone_neuron_differentiation 


id: 35753
description: GO:0021888 Hypothalamus gonadotrophin-releasing hormone neuron development
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0021888
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021888_Hypothalamus_gonadotrophin-releasing_hormone_neuron_development 


id: 35761
description: GO:0021902 Commitment of neuronal cell to specific neuron type in forebrain
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0021902
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021902_Commitment_of_neuronal_cell_to_specific_neuron_type_in_forebrain 


id: 35764
description: GO:0021910 Smoothened signaling pathway involved in ventral spinal cord patterning
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0021910
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021910_Smoothened_signaling_pathway_involved_in_ventral_spinal_cord_patterning 


id: 35769
description: GO:0021936 Regulation of cerebellar granule cell precursor proliferation
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0021936
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021936_Regulation_of_cerebellar_granule_cell_precursor_proliferation 


id: 35770
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0021937
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021937_Cerebellar_purkinje_cell-granule_cell_precursor_cell_signaling_involved_in_regulation_of_granule_cell_precursor_cell_proliferation 

description:
  GO:0021937 Cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation 


id: 35771
description: GO:0021940 Positive regulation of cerebellar granule cell precursor proliferation
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0021940
name:
  GOBP_clfamiliaris_ens_gskb_GO:0021940_Positive_regulation_of_cerebellar_granule_cell_precursor_proliferation 


id: 35798
description: GO:0022028 Tangential migration from the subventricular zone to the olfactory bulb
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0022028
name:
  GOBP_clfamiliaris_ens_gskb_GO:0022028_Tangential_migration_from_the_subventricular_zone_to_the_olfactory_bulb 


id: 35814
description: GO:0022412 Cellular process involved in reproduction in multicellular organism
n: 270
memo: https://amigo.geneontology.org/amigo/term/GO:0022412
name:
  GOBP_clfamiliaris_ens_gskb_GO:0022412_Cellular_process_involved_in_reproduction_in_multicellular_organism 


id: 35832
description: GO:0023019 Signal transduction involved in regulation of gene expression
n: 16
memo: https://amigo.geneontology.org/amigo/term/GO:0023019
name:
  GOBP_clfamiliaris_ens_gskb_GO:0023019_Signal_transduction_involved_in_regulation_of_gene_expression 


id: 35956
description: GO:0030330 Dna damage response signal transduction by p53 class mediator
n: 52
memo: https://amigo.geneontology.org/amigo/term/GO:0030330
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030330_Dna_damage_response_signal_transduction_by_p53_class_mediator 


id: 35979
description: GO:0030511 Positive regulation of transforming growth factor beta receptor signaling pathway
n: 25
memo: https://amigo.geneontology.org/amigo/term/GO:0030511
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030511_Positive_regulation_of_transforming_growth_factor_beta_receptor_signaling_pathway 


id: 35980
description: GO:0030512 Negative regulation of transforming growth factor beta receptor signaling pathway
n: 61
memo: https://amigo.geneontology.org/amigo/term/GO:0030512
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030512_Negative_regulation_of_transforming_growth_factor_beta_receptor_signaling_pathway 


id: 36020
description: GO:0030845 Phospholipase c-inhibiting g protein-coupled receptor signaling pathway
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0030845
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030845_Phospholipase_c-inhibiting_g_protein-coupled_receptor_signaling_pathway 


id: 36021
description: GO:0030846 Termination of rna polymerase ii transcription poly(a)-coupled
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0030846
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030846_Termination_of_rna_polymerase_ii_transcription_poly(a)-coupled 


id: 36050
description: GO:0030947 Regulation of vascular endothelial growth factor receptor signaling pathway
n: 17
memo: https://amigo.geneontology.org/amigo/term/GO:0030947
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030947_Regulation_of_vascular_endothelial_growth_factor_receptor_signaling_pathway 


id: 36051
description: GO:0030948 Negative regulation of vascular endothelial growth factor receptor signaling pathway
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0030948
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030948_Negative_regulation_of_vascular_endothelial_growth_factor_receptor_signaling_pathway 


id: 36052
description: GO:0030949 Positive regulation of vascular endothelial growth factor receptor signaling pathway
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0030949
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030949_Positive_regulation_of_vascular_endothelial_growth_factor_receptor_signaling_pathway 


id: 36054
description: GO:0030951 Establishment or maintenance of microtubule cytoskeleton polarity
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0030951
name:
  GOBP_clfamiliaris_ens_gskb_GO:0030951_Establishment_or_maintenance_of_microtubule_cytoskeleton_polarity 


id: 36077
description: GO:0031086 Nuclear-transcribed mrna catabolic process deadenylation-independent decay
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0031086
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031086_Nuclear-transcribed_mrna_catabolic_process_deadenylation-independent_decay 


id: 36078
description: GO:0031087 Deadenylation-independent decapping of nuclear-transcribed mrna
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0031087
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031087_Deadenylation-independent_decapping_of_nuclear-transcribed_mrna 


id: 36086
description: GO:0031111 Negative regulation of microtubule polymerization or depolymerization
n: 24
memo: https://amigo.geneontology.org/amigo/term/GO:0031111
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031111_Negative_regulation_of_microtubule_polymerization_or_depolymerization 


id: 36087
description: GO:0031112 Positive regulation of microtubule polymerization or depolymerization
n: 21
memo: https://amigo.geneontology.org/amigo/term/GO:0031112
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031112_Positive_regulation_of_microtubule_polymerization_or_depolymerization 


id: 36104
description: GO:0031146 Scf-dependent proteasomal ubiquitin-dependent protein catabolic process
n: 36
memo: https://amigo.geneontology.org/amigo/term/GO:0031146
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031146_Scf-dependent_proteasomal_ubiquitin-dependent_protein_catabolic_process 


id: 36109
description: GO:0031204 Post-translational protein targeting to membrane translocation
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0031204
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031204_Post-translational_protein_targeting_to_membrane_translocation 


id: 36162
description: GO:0031448 Positive regulation of fast-twitch skeletal muscle fiber contraction
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0031448
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031448_Positive_regulation_of_fast-twitch_skeletal_muscle_fiber_contraction 


id: 36188
description: GO:0031630 Regulation of synaptic vesicle fusion to presynaptic active zone membrane
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0031630
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031630_Regulation_of_synaptic_vesicle_fusion_to_presynaptic_active_zone_membrane 


id: 36189
description: GO:0031632 Positive regulation of synaptic vesicle fusion to presynaptic active zone membrane
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0031632
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031632_Positive_regulation_of_synaptic_vesicle_fusion_to_presynaptic_active_zone_membrane 


id: 36206
description: GO:0031665 Negative regulation of lipopolysaccharide-mediated signaling pathway
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0031665
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031665_Negative_regulation_of_lipopolysaccharide-mediated_signaling_pathway 


id: 36207
description: GO:0031666 Positive regulation of lipopolysaccharide-mediated signaling pathway
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0031666
name:
  GOBP_clfamiliaris_ens_gskb_GO:0031666_Positive_regulation_of_lipopolysaccharide-mediated_signaling_pathway 


id: 36282
description: GO:0032240 Negative regulation of nucleobase-containing compound transport
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0032240
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032240_Negative_regulation_of_nucleobase-containing_compound_transport 


id: 36283
description: GO:0032241 Positive regulation of nucleobase-containing compound transport
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0032241
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032241_Positive_regulation_of_nucleobase-containing_compound_transport 


id: 36305
description: GO:0032298 Positive regulation of dna-templated dna replication initiation
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0032298
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032298_Positive_regulation_of_dna-templated_dna_replication_initiation 


id: 36361
description: GO:0032434 Regulation of proteasomal ubiquitin-dependent protein catabolic process
n: 94
memo: https://amigo.geneontology.org/amigo/term/GO:0032434
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032434_Regulation_of_proteasomal_ubiquitin-dependent_protein_catabolic_process 


id: 36362
description: GO:0032435 Negative regulation of proteasomal ubiquitin-dependent protein catabolic process
n: 26
memo: https://amigo.geneontology.org/amigo/term/GO:0032435
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032435_Negative_regulation_of_proteasomal_ubiquitin-dependent_protein_catabolic_process 


id: 36363
description: GO:0032436 Positive regulation of proteasomal ubiquitin-dependent protein catabolic process
n: 59
memo: https://amigo.geneontology.org/amigo/term/GO:0032436
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032436_Positive_regulation_of_proteasomal_ubiquitin-dependent_protein_catabolic_process 


id: 36377
description: GO:0032470 Positive regulation of endoplasmic reticulum calcium ion concentration
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0032470
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032470_Positive_regulation_of_endoplasmic_reticulum_calcium_ion_concentration 


id: 36378
description: GO:0032471 Negative regulation of endoplasmic reticulum calcium ion concentration
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0032471
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032471_Negative_regulation_of_endoplasmic_reticulum_calcium_ion_concentration 


id: 36404
description: GO:0032510 Endosome to lysosome transport via multivesicular body sorting pathway
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0032510
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032510_Endosome_to_lysosome_transport_via_multivesicular_body_sorting_pathway 


id: 36405
description: GO:0032511 Late endosome to vacuole transport via multivesicular body sorting pathway
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0032511
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032511_Late_endosome_to_vacuole_transport_via_multivesicular_body_sorting_pathway 


id: 36443
description: GO:0032645 Regulation of granulocyte macrophage colony-stimulating factor production
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0032645
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032645_Regulation_of_granulocyte_macrophage_colony-stimulating_factor_production 


id: 36482
description: GO:0032725 Positive regulation of granulocyte macrophage colony-stimulating factor production
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0032725
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032725_Positive_regulation_of_granulocyte_macrophage_colony-stimulating_factor_production 


id: 36507
description: GO:0032785 Negative regulation of dna-templated transcription elongation
n: 15
memo: https://amigo.geneontology.org/amigo/term/GO:0032785
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032785_Negative_regulation_of_dna-templated_transcription_elongation 


id: 36508
description: GO:0032786 Positive regulation of dna-templated transcription elongation
n: 21
memo: https://amigo.geneontology.org/amigo/term/GO:0032786
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032786_Positive_regulation_of_dna-templated_transcription_elongation 


id: 36515
description: GO:0032803 Regulation of low-density lipoprotein particle receptor catabolic process
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0032803
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032803_Regulation_of_low-density_lipoprotein_particle_receptor_catabolic_process 


id: 36516
description: GO:0032804 Negative regulation of low-density lipoprotein particle receptor catabolic process
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0032804
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032804_Negative_regulation_of_low-density_lipoprotein_particle_receptor_catabolic_process 


id: 36526
description: GO:0032826 Regulation of natural killer cell differentiation involved in immune response
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0032826
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032826_Regulation_of_natural_killer_cell_differentiation_involved_in_immune_response 


id: 36527
description: GO:0032827 Negative regulation of natural killer cell differentiation involved in immune response
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0032827
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032827_Negative_regulation_of_natural_killer_cell_differentiation_involved_in_immune_response 


id: 36528
description: GO:0032829 Regulation of cd4-positive cd25-positive alpha-beta regulatory t cell differentiation
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0032829
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032829_Regulation_of_cd4-positive_cd25-positive_alpha-beta_regulatory_t_cell_differentiation 


id: 36529
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0032831
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032831_Positive_regulation_of_cd4-positive_cd25-positive_alpha-beta_regulatory_t_cell_differentiation 

description:
  GO:0032831 Positive regulation of cd4-positive cd25-positive alpha-beta regulatory t cell differentiation 


id: 36557
description: GO:0032911 Negative regulation of transforming growth factor beta1 production
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0032911
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032911_Negative_regulation_of_transforming_growth_factor_beta1_production 


id: 36558
description: GO:0032914 Positive regulation of transforming growth factor beta1 production
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0032914
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032914_Positive_regulation_of_transforming_growth_factor_beta1_production 


id: 36559
description: GO:0032915 Positive regulation of transforming growth factor beta2 production
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0032915
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032915_Positive_regulation_of_transforming_growth_factor_beta2_production 


id: 36582
description: GO:0032962 Positive regulation of inositol trisphosphate biosynthetic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0032962
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032962_Positive_regulation_of_inositol_trisphosphate_biosynthetic_process 


id: 36588
description: GO:0032968 Positive regulation of transcription elongation by rna polymerase ii
n: 15
memo: https://amigo.geneontology.org/amigo/term/GO:0032968
name:
  GOBP_clfamiliaris_ens_gskb_GO:0032968_Positive_regulation_of_transcription_elongation_by_rna_polymerase_ii 


id: 36600
description: GO:0033006 Regulation of mast cell activation involved in immune response
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0033006
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033006_Regulation_of_mast_cell_activation_involved_in_immune_response 


id: 36601
description: GO:0033007 Negative regulation of mast cell activation involved in immune response
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0033007
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033007_Negative_regulation_of_mast_cell_activation_involved_in_immune_response 


id: 36632
description: GO:0033088 Negative regulation of immature t cell proliferation in thymus
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0033088
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033088_Negative_regulation_of_immature_t_cell_proliferation_in_thymus 


id: 36635
description: GO:0033092 Positive regulation of immature t cell proliferation in thymus
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0033092
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033092_Positive_regulation_of_immature_t_cell_proliferation_in_thymus 


id: 36645
description: GO:0033139 Regulation of peptidyl-serine phosphorylation of stat protein
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0033139
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033139_Regulation_of_peptidyl-serine_phosphorylation_of_stat_protein 


id: 36646
description: GO:0033140 Negative regulation of peptidyl-serine phosphorylation of stat protein
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0033140
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033140_Negative_regulation_of_peptidyl-serine_phosphorylation_of_stat_protein 


id: 36647
description: GO:0033143 Regulation of intracellular steroid hormone receptor signaling pathway
n: 50
memo: https://amigo.geneontology.org/amigo/term/GO:0033143
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033143_Regulation_of_intracellular_steroid_hormone_receptor_signaling_pathway 


id: 36648
description: GO:0033144 Negative regulation of intracellular steroid hormone receptor signaling pathway
n: 27
memo: https://amigo.geneontology.org/amigo/term/GO:0033144
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033144_Negative_regulation_of_intracellular_steroid_hormone_receptor_signaling_pathway 


id: 36649
description: GO:0033145 Positive regulation of intracellular steroid hormone receptor signaling pathway
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0033145
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033145_Positive_regulation_of_intracellular_steroid_hormone_receptor_signaling_pathway 


id: 36650
description: GO:0033146 Regulation of intracellular estrogen receptor signaling pathway
n: 26
memo: https://amigo.geneontology.org/amigo/term/GO:0033146
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033146_Regulation_of_intracellular_estrogen_receptor_signaling_pathway 


id: 36651
description: GO:0033147 Negative regulation of intracellular estrogen receptor signaling pathway
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0033147
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033147_Negative_regulation_of_intracellular_estrogen_receptor_signaling_pathway 


id: 36652
description: GO:0033148 Positive regulation of intracellular estrogen receptor signaling pathway
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0033148
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033148_Positive_regulation_of_intracellular_estrogen_receptor_signaling_pathway 


id: 36707
description: GO:0033600 Negative regulation of mammary gland epithelial cell proliferation
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0033600
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033600_Negative_regulation_of_mammary_gland_epithelial_cell_proliferation 


id: 36708
description: GO:0033601 Positive regulation of mammary gland epithelial cell proliferation
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0033601
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033601_Positive_regulation_of_mammary_gland_epithelial_cell_proliferation 


id: 36711
description: GO:0033615 Mitochondrial proton-transporting atp synthase complex assembly
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0033615
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033615_Mitochondrial_proton-transporting_atp_synthase_complex_assembly 


id: 36724
description: GO:0033633 Negative regulation of cell-cell adhesion mediated by integrin
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0033633
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033633_Negative_regulation_of_cell-cell_adhesion_mediated_by_integrin 


id: 36725
description: GO:0033634 Positive regulation of cell-cell adhesion mediated by integrin
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0033634
name:
  GOBP_clfamiliaris_ens_gskb_GO:0033634_Positive_regulation_of_cell-cell_adhesion_mediated_by_integrin 


id: 36755
description: GO:0034093 Positive regulation of maintenance of sister chromatid cohesion
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0034093
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034093_Positive_regulation_of_maintenance_of_sister_chromatid_cohesion 


id: 36774
description: GO:0034136 Negative regulation of toll-like receptor 2 signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0034136
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034136_Negative_regulation_of_toll-like_receptor_2_signaling_pathway 


id: 36775
description: GO:0034137 Positive regulation of toll-like receptor 2 signaling pathway
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0034137
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034137_Positive_regulation_of_toll-like_receptor_2_signaling_pathway 


id: 36778
description: GO:0034140 Negative regulation of toll-like receptor 3 signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0034140
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034140_Negative_regulation_of_toll-like_receptor_3_signaling_pathway 


id: 36779
description: GO:0034141 Positive regulation of toll-like receptor 3 signaling pathway
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0034141
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034141_Positive_regulation_of_toll-like_receptor_3_signaling_pathway 


id: 36782
description: GO:0034144 Negative regulation of toll-like receptor 4 signaling pathway
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0034144
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034144_Negative_regulation_of_toll-like_receptor_4_signaling_pathway 


id: 36783
description: GO:0034145 Positive regulation of toll-like receptor 4 signaling pathway
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0034145
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034145_Positive_regulation_of_toll-like_receptor_4_signaling_pathway 


id: 36787
description: GO:0034157 Positive regulation of toll-like receptor 7 signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0034157
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034157_Positive_regulation_of_toll-like_receptor_7_signaling_pathway 


id: 36790
description: GO:0034161 Positive regulation of toll-like receptor 8 signaling pathway
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0034161
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034161_Positive_regulation_of_toll-like_receptor_8_signaling_pathway 


id: 36793
description: GO:0034164 Negative regulation of toll-like receptor 9 signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0034164
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034164_Negative_regulation_of_toll-like_receptor_9_signaling_pathway 


id: 36794
description: GO:0034165 Positive regulation of toll-like receptor 9 signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0034165
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034165_Positive_regulation_of_toll-like_receptor_9_signaling_pathway 


id: 36795
description: GO:0034182 Regulation of maintenance of mitotic sister chromatid cohesion
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0034182
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034182_Regulation_of_maintenance_of_mitotic_sister_chromatid_cohesion 


id: 36796
description: GO:0034184 Positive regulation of maintenance of mitotic sister chromatid cohesion
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0034184
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034184_Positive_regulation_of_maintenance_of_mitotic_sister_chromatid_cohesion 


id: 36811
description: GO:0034242 Negative regulation of syncytium formation by plasma membrane fusion
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0034242
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034242_Negative_regulation_of_syncytium_formation_by_plasma_membrane_fusion 


id: 36813
description: GO:0034244 Negative regulation of transcription elongation by rna polymerase ii
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0034244
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034244_Negative_regulation_of_transcription_elongation_by_rna_polymerase_ii 


id: 36826
description: GO:0034316 Negative regulation of arp2/3 complex-mediated actin nucleation
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0034316
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034316_Negative_regulation_of_arp2/3_complex-mediated_actin_nucleation 


id: 36909
description: GO:0034643 Establishment of mitochondrion localization microtubule-mediated
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0034643
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034643_Establishment_of_mitochondrion_localization_microtubule-mediated 


id: 36929
description: GO:0034766 Negative regulation of monoatomic ion transmembrane transport
n: 23
memo: https://amigo.geneontology.org/amigo/term/GO:0034766
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034766_Negative_regulation_of_monoatomic_ion_transmembrane_transport 


id: 36930
description: GO:0034767 Positive regulation of monoatomic ion transmembrane transport
n: 36
memo: https://amigo.geneontology.org/amigo/term/GO:0034767
name:
  GOBP_clfamiliaris_ens_gskb_GO:0034767_Positive_regulation_of_monoatomic_ion_transmembrane_transport 


id: 36946
description: GO:0035054 Embryonic heart tube anterior/posterior pattern specification
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0035054
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035054_Embryonic_heart_tube_anterior/posterior_pattern_specification 


id: 36972
description: GO:0035194 Regulatory ncrna-mediated post-transcriptional gene silencing
n: 42
memo: https://amigo.geneontology.org/amigo/term/GO:0035194
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035194_Regulatory_ncrna-mediated_post-transcriptional_gene_silencing 


id: 37015
description: GO:0035358 Regulation of peroxisome proliferator activated receptor signaling pathway
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0035358
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035358_Regulation_of_peroxisome_proliferator_activated_receptor_signaling_pathway 


id: 37016
description: GO:0035359 Negative regulation of peroxisome proliferator activated receptor signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0035359
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035359_Negative_regulation_of_peroxisome_proliferator_activated_receptor_signaling_pathway 


id: 37017
description: GO:0035360 Positive regulation of peroxisome proliferator activated receptor signaling pathway
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0035360
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035360_Positive_regulation_of_peroxisome_proliferator_activated_receptor_signaling_pathway 


id: 37062
description: GO:0035589 G protein-coupled purinergic nucleotide receptor signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0035589
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035589_G_protein-coupled_purinergic_nucleotide_receptor_signaling_pathway 


id: 37064
description: GO:0035592 Establishment of protein localization to extracellular region
n: 230
memo: https://amigo.geneontology.org/amigo/term/GO:0035592
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035592_Establishment_of_protein_localization_to_extracellular_region 


id: 37119
description: GO:0035773 Insulin secretion involved in cellular response to glucose stimulus
n: 43
memo: https://amigo.geneontology.org/amigo/term/GO:0035773
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035773_Insulin_secretion_involved_in_cellular_response_to_glucose_stimulus 


id: 37120
n: 20
memo: https://amigo.geneontology.org/amigo/term/GO:0035774
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035774_Positive_regulation_of_insulin_secretion_involved_in_cellular_response_to_glucose_stimulus 

description:
  GO:0035774 Positive regulation of insulin secretion involved in cellular response to glucose stimulus 


id: 37125
description: GO:0035790 Platelet-derived growth factor receptor-alpha signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0035790
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035790_Platelet-derived_growth_factor_receptor-alpha_signaling_pathway 


id: 37126
description: GO:0035791 Platelet-derived growth factor receptor-beta signaling pathway
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0035791
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035791_Platelet-derived_growth_factor_receptor-beta_signaling_pathway 


id: 37145
description: GO:0035850 Epithelial cell differentiation involved in kidney development
n: 38
memo: https://amigo.geneontology.org/amigo/term/GO:0035850
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035850_Epithelial_cell_differentiation_involved_in_kidney_development 


id: 37148
description: GO:0035860 Glial cell-derived neurotrophic factor receptor signaling pathway
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0035860
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035860_Glial_cell-derived_neurotrophic_factor_receptor_signaling_pathway 


id: 37152
description: GO:0035872 Nucleotide-binding domain leucine rich repeat containing receptor signaling pathway
n: 16
memo: https://amigo.geneontology.org/amigo/term/GO:0035872
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035872_Nucleotide-binding_domain_leucine_rich_repeat_containing_receptor_signaling_pathway 


id: 37168
description: GO:0035924 Cellular response to vascular endothelial growth factor stimulus
n: 49
memo: https://amigo.geneontology.org/amigo/term/GO:0035924
name:
  GOBP_clfamiliaris_ens_gskb_GO:0035924_Cellular_response_to_vascular_endothelial_growth_factor_stimulus 


id: 37194
description: GO:0036006 Cellular response to macrophage colony-stimulating factor stimulus
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0036006
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036006_Cellular_response_to_macrophage_colony-stimulating_factor_stimulus 


id: 37254
description: GO:0036324 Vascular endothelial growth factor receptor-2 signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0036324
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036324_Vascular_endothelial_growth_factor_receptor-2_signaling_pathway 


id: 37275
description: GO:0036480 Neuron intrinsic apoptotic signaling pathway in response to oxidative stress
n: 15
memo: https://amigo.geneontology.org/amigo/term/GO:0036480
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036480_Neuron_intrinsic_apoptotic_signaling_pathway_in_response_to_oxidative_stress 


id: 37276
description: GO:0036481 Intrinsic apoptotic signaling pathway in response to hydrogen peroxide
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0036481
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036481_Intrinsic_apoptotic_signaling_pathway_in_response_to_hydrogen_peroxide 


id: 37277
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0036483
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036483_Neuron_intrinsic_apoptotic_signaling_pathway_in_response_to_endoplasmic_reticulum_stress 

description:
  GO:0036483 Neuron intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress 


id: 37280
description: GO:0036490 Regulation of translation in response to endoplasmic reticulum stress
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0036490
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036490_Regulation_of_translation_in_response_to_endoplasmic_reticulum_stress 


id: 37281
description: GO:0036491 Regulation of translation initiation in response to endoplasmic reticulum stress
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0036491
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036491_Regulation_of_translation_initiation_in_response_to_endoplasmic_reticulum_stress 


id: 37282
description: GO:0036492 Eif2alpha phosphorylation in response to endoplasmic reticulum stress
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0036492
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036492_Eif2alpha_phosphorylation_in_response_to_endoplasmic_reticulum_stress 


id: 37283
description: GO:0036493 Positive regulation of translation in response to endoplasmic reticulum stress
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0036493
name:
  GOBP_clfamiliaris_ens_gskb_GO:0036493_Positive_regulation_of_translation_in_response_to_endoplasmic_reticulum_stress 


id: 37304
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0038035
name:
  GOBP_clfamiliaris_ens_gskb_GO:0038035_Ligand-independent_adenylate_cyclase-activating_g_protein-coupled_receptor_signaling_pathway 

description:
  GO:0038035 Ligand-independent adenylate cyclase-activating g protein-coupled receptor signaling pathway 


id: 37308
description: GO:0038063 Collagen-activated tyrosine kinase receptor signaling pathway
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0038063
name:
  GOBP_clfamiliaris_ens_gskb_GO:0038063_Collagen-activated_tyrosine_kinase_receptor_signaling_pathway 


id: 37313
description: GO:0038086 Vegf-activated platelet-derived growth factor receptor signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0038086
name:
  GOBP_clfamiliaris_ens_gskb_GO:0038086_Vegf-activated_platelet-derived_growth_factor_receptor_signaling_pathway 


id: 37314
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0038091
name:
  GOBP_clfamiliaris_ens_gskb_GO:0038091_Positive_regulation_of_cell_proliferation_by_vegf-activated_platelet_derived_growth_factor_receptor_signaling_pathway 

description:
  GO:0038091 Positive regulation of cell proliferation by vegf-activated platelet derived growth factor receptor signaling pathway 


id: 37321
description: GO:0038108 Negative regulation of appetite by leptin-mediated signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0038108
name:
  GOBP_clfamiliaris_ens_gskb_GO:0038108_Negative_regulation_of_appetite_by_leptin-mediated_signaling_pathway 


id: 37341
description: GO:0038157 Granulocyte-macrophage colony-stimulating factor signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0038157
name:
  GOBP_clfamiliaris_ens_gskb_GO:0038157_Granulocyte-macrophage_colony-stimulating_factor_signaling_pathway 


id: 37366
description: GO:0039531 Regulation of cytoplasmic pattern recognition receptor signaling pathway
n: 81
memo: https://amigo.geneontology.org/amigo/term/GO:0039531
name:
  GOBP_clfamiliaris_ens_gskb_GO:0039531_Regulation_of_cytoplasmic_pattern_recognition_receptor_signaling_pathway 


id: 37367
description: GO:0039532 Negative regulation of cytoplasmic pattern recognition receptor signaling pathway
n: 44
memo: https://amigo.geneontology.org/amigo/term/GO:0039532
name:
  GOBP_clfamiliaris_ens_gskb_GO:0039532_Negative_regulation_of_cytoplasmic_pattern_recognition_receptor_signaling_pathway 


id: 37374
description: GO:0039692 Single stranded viral rna replication via double stranded dna intermediate
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0039692
name:
  GOBP_clfamiliaris_ens_gskb_GO:0039692_Single_stranded_viral_rna_replication_via_double_stranded_dna_intermediate 


id: 37394
description: GO:0040036 Regulation of fibroblast growth factor receptor signaling pathway
n: 22
memo: https://amigo.geneontology.org/amigo/term/GO:0040036
name:
  GOBP_clfamiliaris_ens_gskb_GO:0040036_Regulation_of_fibroblast_growth_factor_receptor_signaling_pathway 


id: 37395
description: GO:0040037 Negative regulation of fibroblast growth factor receptor signaling pathway
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0040037
name:
  GOBP_clfamiliaris_ens_gskb_GO:0040037_Negative_regulation_of_fibroblast_growth_factor_receptor_signaling_pathway 


id: 37404
description: GO:0042058 Regulation of epidermal growth factor receptor signaling pathway
n: 44
memo: https://amigo.geneontology.org/amigo/term/GO:0042058
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042058_Regulation_of_epidermal_growth_factor_receptor_signaling_pathway 


id: 37405
description: GO:0042059 Negative regulation of epidermal growth factor receptor signaling pathway
n: 17
memo: https://amigo.geneontology.org/amigo/term/GO:0042059
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042059_Negative_regulation_of_epidermal_growth_factor_receptor_signaling_pathway 


id: 37533
description: GO:0042488 Positive regulation of odontogenesis of dentin-containing tooth
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0042488
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042488_Positive_regulation_of_odontogenesis_of_dentin-containing_tooth 


id: 37534
description: GO:0042489 Negative regulation of odontogenesis of dentin-containing tooth
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0042489
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042489_Negative_regulation_of_odontogenesis_of_dentin-containing_tooth 


id: 37542
description: GO:0042531 Positive regulation of tyrosine phosphorylation of stat protein
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0042531
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042531_Positive_regulation_of_tyrosine_phosphorylation_of_stat_protein 


id: 37543
description: GO:0042532 Negative regulation of tyrosine phosphorylation of stat protein
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0042532
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042532_Negative_regulation_of_tyrosine_phosphorylation_of_stat_protein 


id: 37603
description: GO:0042771 Intrinsic apoptotic signaling pathway in response to dna damage by p53 class mediator
n: 30
memo: https://amigo.geneontology.org/amigo/term/GO:0042771
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042771_Intrinsic_apoptotic_signaling_pathway_in_response_to_dna_damage_by_p53_class_mediator 


id: 37604
description: GO:0042772 Dna damage response signal transduction resulting in transcription
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0042772
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042772_Dna_damage_response_signal_transduction_resulting_in_transcription 


id: 37641
description: GO:0042985 Negative regulation of amyloid precursor protein biosynthetic process
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0042985
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042985_Negative_regulation_of_amyloid_precursor_protein_biosynthetic_process 


id: 37642
description: GO:0042986 Positive regulation of amyloid precursor protein biosynthetic process
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0042986
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042986_Positive_regulation_of_amyloid_precursor_protein_biosynthetic_process 


id: 37646
description: GO:0042997 Negative regulation of golgi to plasma membrane protein transport
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0042997
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042997_Negative_regulation_of_golgi_to_plasma_membrane_protein_transport 


id: 37647
description: GO:0042998 Positive regulation of golgi to plasma membrane protein transport
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0042998
name:
  GOBP_clfamiliaris_ens_gskb_GO:0042998_Positive_regulation_of_golgi_to_plasma_membrane_protein_transport 


id: 37679
description: GO:0043123 Positive regulation of canonical nf-kappab signal transduction
n: 126
memo: https://amigo.geneontology.org/amigo/term/GO:0043123
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043123_Positive_regulation_of_canonical_nf-kappab_signal_transduction 


id: 37680
description: GO:0043124 Negative regulation of canonical nf-kappab signal transduction
n: 45
memo: https://amigo.geneontology.org/amigo/term/GO:0043124
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043124_Negative_regulation_of_canonical_nf-kappab_signal_transduction 


id: 37688
description: GO:0043161 Proteasome-mediated ubiquitin-dependent protein catabolic process
n: 281
memo: https://amigo.geneontology.org/amigo/term/GO:0043161
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043161_Proteasome-mediated_ubiquitin-dependent_protein_catabolic_process 


id: 37689
n: 24
memo: https://amigo.geneontology.org/amigo/term/GO:0043162
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043162_Ubiquitin-dependent_protein_catabolic_process_via_the_multivesicular_body_sorting_pathway 

description:
  GO:0043162 Ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway 


id: 37698
description: GO:0043242 Negative regulation of protein-containing complex disassembly
n: 52
memo: https://amigo.geneontology.org/amigo/term/GO:0043242
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043242_Negative_regulation_of_protein-containing_complex_disassembly 


id: 37699
description: GO:0043243 Positive regulation of protein-containing complex disassembly
n: 25
memo: https://amigo.geneontology.org/amigo/term/GO:0043243
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043243_Positive_regulation_of_protein-containing_complex_disassembly 


id: 37735
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0043328
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043328_Protein_transport_to_vacuole_involved_in_ubiquitin-dependent_protein_catabolic_process_via_the_multivesicular_body_sorting_pathway 

description:
  GO:0043328 Protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway 


id: 37744
description: GO:0043369 Cd4-positive or cd8-positive alpha-beta t cell lineage commitment
n: 19
memo: https://amigo.geneontology.org/amigo/term/GO:0043369
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043369_Cd4-positive_or_cd8-positive_alpha-beta_t_cell_lineage_commitment 


id: 37746
description: GO:0043371 Negative regulation of cd4-positive alpha-beta t cell differentiation
n: 19
memo: https://amigo.geneontology.org/amigo/term/GO:0043371
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043371_Negative_regulation_of_cd4-positive_alpha-beta_t_cell_differentiation 


id: 37747
description: GO:0043372 Positive regulation of cd4-positive alpha-beta t cell differentiation
n: 22
memo: https://amigo.geneontology.org/amigo/term/GO:0043372
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043372_Positive_regulation_of_cd4-positive_alpha-beta_t_cell_differentiation 


id: 37791
description: GO:0043491 Phosphatidylinositol 3-kinase/protein kinase b signal transduction
n: 201
memo: https://amigo.geneontology.org/amigo/term/GO:0043491
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043491_Phosphatidylinositol_3-kinase/protein_kinase_b_signal_transduction 


id: 37797
description: GO:0043516 Regulation of dna damage response signal transduction by p53 class mediator
n: 28
memo: https://amigo.geneontology.org/amigo/term/GO:0043516
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043516_Regulation_of_dna_damage_response_signal_transduction_by_p53_class_mediator 


id: 37798
description: GO:0043517 Positive regulation of dna damage response signal transduction by p53 class mediator
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0043517
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043517_Positive_regulation_of_dna_damage_response_signal_transduction_by_p53_class_mediator 


id: 37799
description: GO:0043518 Negative regulation of dna damage response signal transduction by p53 class mediator
n: 11
memo: https://amigo.geneontology.org/amigo/term/GO:0043518
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043518_Negative_regulation_of_dna_damage_response_signal_transduction_by_p53_class_mediator 


id: 37805
description: GO:0043536 Positive regulation of blood vessel endothelial cell migration
n: 42
memo: https://amigo.geneontology.org/amigo/term/GO:0043536
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043536_Positive_regulation_of_blood_vessel_endothelial_cell_migration 


id: 37806
description: GO:0043537 Negative regulation of blood vessel endothelial cell migration
n: 28
memo: https://amigo.geneontology.org/amigo/term/GO:0043537
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043537_Negative_regulation_of_blood_vessel_endothelial_cell_migration 


id: 37814
description: GO:0043567 Regulation of insulin-like growth factor receptor signaling pathway
n: 16
memo: https://amigo.geneontology.org/amigo/term/GO:0043567
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043567_Regulation_of_insulin-like_growth_factor_receptor_signaling_pathway 


id: 37815
description: GO:0043568 Positive regulation of insulin-like growth factor receptor signaling pathway
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0043568
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043568_Positive_regulation_of_insulin-like_growth_factor_receptor_signaling_pathway 


id: 37816
description: GO:0043569 Negative regulation of insulin-like growth factor receptor signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0043569
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043569_Negative_regulation_of_insulin-like_growth_factor_receptor_signaling_pathway 


id: 37849
description: GO:0043903 Regulation of biological process involved in symbiotic interaction
n: 30
memo: https://amigo.geneontology.org/amigo/term/GO:0043903
name:
  GOBP_clfamiliaris_ens_gskb_GO:0043903_Regulation_of_biological_process_involved_in_symbiotic_interaction 


id: 37859
description: GO:0044027 Negative regulation of gene expression via chromosomal cpg island methylation
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0044027
name:
  GOBP_clfamiliaris_ens_gskb_GO:0044027_Negative_regulation_of_gene_expression_via_chromosomal_cpg_island_methylation 


id: 37860
description: GO:0044029 Positive regulation of gene expression via chromosomal cpg island demethylation
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0044029
name:
  GOBP_clfamiliaris_ens_gskb_GO:0044029_Positive_regulation_of_gene_expression_via_chromosomal_cpg_island_demethylation 


id: 37900
description: GO:0044338 Canonical wnt signaling pathway involved in mesenchymal stem cell differentiation
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0044338
name:
  GOBP_clfamiliaris_ens_gskb_GO:0044338_Canonical_wnt_signaling_pathway_involved_in_mesenchymal_stem_cell_differentiation 


id: 37913
description: GO:0044419 Biological process involved in interspecies interaction between organisms
n: 948
memo: https://amigo.geneontology.org/amigo/term/GO:0044419
name:
  GOBP_clfamiliaris_ens_gskb_GO:0044419_Biological_process_involved_in_interspecies_interaction_between_organisms 


id: 37988
description: GO:0045050 Protein insertion into er membrane by stop-transfer membrane-anchor sequence
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0045050
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045050_Protein_insertion_into_er_membrane_by_stop-transfer_membrane-anchor_sequence 


id: 38006
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0045091
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045091_Regulation_of_single_stranded_viral_rna_replication_via_double_stranded_dna_intermediate 

description:
  GO:0045091 Regulation of single stranded viral rna replication via double stranded dna intermediate 


id: 38034
description: GO:0045197 Establishment or maintenance of epithelial cell apical/basal polarity
n: 39
memo: https://amigo.geneontology.org/amigo/term/GO:0045197
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045197_Establishment_or_maintenance_of_epithelial_cell_apical/basal_polarity 


id: 38098
description: GO:0045607 Regulation of inner ear auditory receptor cell differentiation
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0045607
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045607_Regulation_of_inner_ear_auditory_receptor_cell_differentiation 


id: 38099
description: GO:0045608 Negative regulation of inner ear auditory receptor cell differentiation
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0045608
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045608_Negative_regulation_of_inner_ear_auditory_receptor_cell_differentiation 


id: 38168
description: GO:0045741 Positive regulation of epidermal growth factor-activated receptor activity
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0045741
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045741_Positive_regulation_of_epidermal_growth_factor-activated_receptor_activity 


id: 38169
description: GO:0045742 Positive regulation of epidermal growth factor receptor signaling pathway
n: 19
memo: https://amigo.geneontology.org/amigo/term/GO:0045742
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045742_Positive_regulation_of_epidermal_growth_factor_receptor_signaling_pathway 


id: 38170
description: GO:0045743 Positive regulation of fibroblast growth factor receptor signaling pathway
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0045743
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045743_Positive_regulation_of_fibroblast_growth_factor_receptor_signaling_pathway 


id: 38171
description: GO:0045744 Negative regulation of g protein-coupled receptor signaling pathway
n: 36
memo: https://amigo.geneontology.org/amigo/term/GO:0045744
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045744_Negative_regulation_of_g_protein-coupled_receptor_signaling_pathway 


id: 38172
description: GO:0045745 Positive regulation of g protein-coupled receptor signaling pathway
n: 22
memo: https://amigo.geneontology.org/amigo/term/GO:0045745
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045745_Positive_regulation_of_g_protein-coupled_receptor_signaling_pathway 


id: 38222
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0045869
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045869_Negative_regulation_of_single_stranded_viral_rna_replication_via_double_stranded_dna_intermediate 

description:
  GO:0045869 Negative regulation of single stranded viral rna replication via double stranded dna intermediate 


id: 38223
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0045870
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045870_Positive_regulation_of_single_stranded_viral_rna_replication_via_double_stranded_dna_intermediate 

description:
  GO:0045870 Positive regulation of single stranded viral rna replication via double stranded dna intermediate 


id: 38230
description: GO:0045898 Regulation of rna polymerase ii transcription preinitiation complex assembly
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0045898
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045898_Regulation_of_rna_polymerase_ii_transcription_preinitiation_complex_assembly 


id: 38231
description: GO:0045899 Positive regulation of rna polymerase ii transcription preinitiation complex assembly
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0045899
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045899_Positive_regulation_of_rna_polymerase_ii_transcription_preinitiation_complex_assembly 


id: 38254
description: GO:0045934 Negative regulation of nucleobase-containing compound metabolic process
n: 1043
memo: https://amigo.geneontology.org/amigo/term/GO:0045934
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045934_Negative_regulation_of_nucleobase-containing_compound_metabolic_process 


id: 38255
description: GO:0045935 Positive regulation of nucleobase-containing compound metabolic process
n: 1417
memo: https://amigo.geneontology.org/amigo/term/GO:0045935
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045935_Positive_regulation_of_nucleobase-containing_compound_metabolic_process 


id: 38266
description: GO:0045953 Negative regulation of natural killer cell mediated cytotoxicity
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0045953
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045953_Negative_regulation_of_natural_killer_cell_mediated_cytotoxicity 


id: 38267
description: GO:0045954 Positive regulation of natural killer cell mediated cytotoxicity
n: 18
memo: https://amigo.geneontology.org/amigo/term/GO:0045954
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045954_Positive_regulation_of_natural_killer_cell_mediated_cytotoxicity 


id: 38270
description: GO:0045959 Negative regulation of complement activation classical pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0045959
name:
  GOBP_clfamiliaris_ens_gskb_GO:0045959_Negative_regulation_of_complement_activation_classical_pathway 


id: 38397
description: GO:0046426 Negative regulation of receptor signaling pathway via jak-stat
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0046426
name:
  GOBP_clfamiliaris_ens_gskb_GO:0046426_Negative_regulation_of_receptor_signaling_pathway_via_jak-stat 


id: 38398
description: GO:0046427 Positive regulation of receptor signaling pathway via jak-stat
n: 21
memo: https://amigo.geneontology.org/amigo/term/GO:0046427
name:
  GOBP_clfamiliaris_ens_gskb_GO:0046427_Positive_regulation_of_receptor_signaling_pathway_via_jak-stat 


id: 38510
description: GO:0046726 Positive regulation by virus of viral protein levels in host cell
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0046726
name:
  GOBP_clfamiliaris_ens_gskb_GO:0046726_Positive_regulation_by_virus_of_viral_protein_levels_in_host_cell 


id: 38545
description: GO:0046881 Positive regulation of follicle-stimulating hormone secretion
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0046881
name:
  GOBP_clfamiliaris_ens_gskb_GO:0046881_Positive_regulation_of_follicle-stimulating_hormone_secretion 


id: 38578
description: GO:0048003 Antigen processing and presentation of lipid antigen via mhc class ib
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0048003
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048003_Antigen_processing_and_presentation_of_lipid_antigen_via_mhc_class_ib 


id: 38579
description: GO:0048006 Antigen processing and presentation endogenous lipid antigen via mhc class ib
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0048006
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048006_Antigen_processing_and_presentation_endogenous_lipid_antigen_via_mhc_class_ib 


id: 38580
description: GO:0048007 Antigen processing and presentation exogenous lipid antigen via mhc class ib
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0048007
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048007_Antigen_processing_and_presentation_exogenous_lipid_antigen_via_mhc_class_ib 


id: 38583
description: GO:0048010 Vascular endothelial growth factor receptor signaling pathway
n: 33
memo: https://amigo.geneontology.org/amigo/term/GO:0048010
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048010_Vascular_endothelial_growth_factor_receptor_signaling_pathway 


id: 38623
description: GO:0048170 Positive regulation of long-term neuronal synaptic plasticity
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0048170
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048170_Positive_regulation_of_long-term_neuronal_synaptic_plasticity 


id: 38693
description: GO:0048386 Positive regulation of retinoic acid receptor signaling pathway
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0048386
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048386_Positive_regulation_of_retinoic_acid_receptor_signaling_pathway 


id: 38694
description: GO:0048387 Negative regulation of retinoic acid receptor signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0048387
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048387_Negative_regulation_of_retinoic_acid_receptor_signaling_pathway 


id: 38798
description: GO:0048692 Negative regulation of axon extension involved in regeneration
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0048692
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048692_Negative_regulation_of_axon_extension_involved_in_regeneration 


id: 38800
description: GO:0048697 Positive regulation of collateral sprouting in absence of injury
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0048697
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048697_Positive_regulation_of_collateral_sprouting_in_absence_of_injury 


id: 38853
description: GO:0048842 Positive regulation of axon extension involved in axon guidance
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0048842
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048842_Positive_regulation_of_axon_extension_involved_in_axon_guidance 


id: 38854
description: GO:0048843 Negative regulation of axon extension involved in axon guidance
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0048843
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048843_Negative_regulation_of_axon_extension_involved_in_axon_guidance 


id: 38875
description: GO:0048874 Host-mediated regulation of intestinal microbiota composition
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0048874
name:
  GOBP_clfamiliaris_ens_gskb_GO:0048874_Host-mediated_regulation_of_intestinal_microbiota_composition 


id: 38883
description: GO:0050427 3-prime-phosphoadenosine 5-prime-phosphosulfate metabolic process
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0050427
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050427_3-prime-phosphoadenosine_5-prime-phosphosulfate_metabolic_process 


id: 38884
description: GO:0050428 3-prime-phosphoadenosine 5-prime-phosphosulfate biosynthetic process
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0050428
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050428_3-prime-phosphoadenosine_5-prime-phosphosulfate_biosynthetic_process 


id: 38976
description: GO:0050857 Positive regulation of antigen receptor-mediated signaling pathway
n: 19
memo: https://amigo.geneontology.org/amigo/term/GO:0050857
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050857_Positive_regulation_of_antigen_receptor-mediated_signaling_pathway 


id: 38977
description: GO:0050858 Negative regulation of antigen receptor-mediated signaling pathway
n: 23
memo: https://amigo.geneontology.org/amigo/term/GO:0050858
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050858_Negative_regulation_of_antigen_receptor-mediated_signaling_pathway 


id: 39011
description: GO:0050907 Detection of chemical stimulus involved in sensory perception
n: 569
memo: https://amigo.geneontology.org/amigo/term/GO:0050907
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050907_Detection_of_chemical_stimulus_involved_in_sensory_perception 


id: 39014
description: GO:0050910 Detection of mechanical stimulus involved in sensory perception of sound
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0050910
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050910_Detection_of_mechanical_stimulus_involved_in_sensory_perception_of_sound 


id: 39015
description: GO:0050911 Detection of chemical stimulus involved in sensory perception of smell
n: 544
memo: https://amigo.geneontology.org/amigo/term/GO:0050911
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050911_Detection_of_chemical_stimulus_involved_in_sensory_perception_of_smell 


id: 39016
description: GO:0050912 Detection of chemical stimulus involved in sensory perception of taste
n: 22
memo: https://amigo.geneontology.org/amigo/term/GO:0050912
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050912_Detection_of_chemical_stimulus_involved_in_sensory_perception_of_taste 


id: 39039
description: GO:0050961 Detection of temperature stimulus involved in sensory perception
n: 14
memo: https://amigo.geneontology.org/amigo/term/GO:0050961
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050961_Detection_of_temperature_stimulus_involved_in_sensory_perception 


id: 39041
description: GO:0050965 Detection of temperature stimulus involved in sensory perception of pain
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0050965
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050965_Detection_of_temperature_stimulus_involved_in_sensory_perception_of_pain 


id: 39042
description: GO:0050966 Detection of mechanical stimulus involved in sensory perception of pain
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0050966
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050966_Detection_of_mechanical_stimulus_involved_in_sensory_perception_of_pain 


id: 39043
description: GO:0050968 Detection of chemical stimulus involved in sensory perception of pain
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0050968
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050968_Detection_of_chemical_stimulus_involved_in_sensory_perception_of_pain 


id: 39044
description: GO:0050974 Detection of mechanical stimulus involved in sensory perception
n: 24
memo: https://amigo.geneontology.org/amigo/term/GO:0050974
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050974_Detection_of_mechanical_stimulus_involved_in_sensory_perception 


id: 39046
description: GO:0050976 Detection of mechanical stimulus involved in sensory perception of touch
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0050976
name:
  GOBP_clfamiliaris_ens_gskb_GO:0050976_Detection_of_mechanical_stimulus_involved_in_sensory_perception_of_touch 


id: 39063
description: GO:0051044 Positive regulation of membrane protein ectodomain proteolysis
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0051044
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051044_Positive_regulation_of_membrane_protein_ectodomain_proteolysis 


id: 39064
description: GO:0051045 Negative regulation of membrane protein ectodomain proteolysis
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0051045
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051045_Negative_regulation_of_membrane_protein_ectodomain_proteolysis 


id: 39076
description: GO:0051057 Positive regulation of small gtpase mediated signal transduction
n: 47
memo: https://amigo.geneontology.org/amigo/term/GO:0051057
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051057_Positive_regulation_of_small_gtpase_mediated_signal_transduction 


id: 39077
description: GO:0051058 Negative regulation of small gtpase mediated signal transduction
n: 41
memo: https://amigo.geneontology.org/amigo/term/GO:0051058
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051058_Negative_regulation_of_small_gtpase_mediated_signal_transduction 


id: 39163
description: GO:0051279 Regulation of release of sequestered calcium ion into cytosol
n: 38
memo: https://amigo.geneontology.org/amigo/term/GO:0051279
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051279_Regulation_of_release_of_sequestered_calcium_ion_into_cytosol 


id: 39164
description: GO:0051281 Positive regulation of release of sequestered calcium ion into cytosol
n: 18
memo: https://amigo.geneontology.org/amigo/term/GO:0051281
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051281_Positive_regulation_of_release_of_sequestered_calcium_ion_into_cytosol 


id: 39199
description: GO:0051388 Positive regulation of neurotrophin trk receptor signaling pathway
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0051388
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051388_Positive_regulation_of_neurotrophin_trk_receptor_signaling_pathway 


id: 39236
description: GO:0051561 Positive regulation of mitochondrial calcium ion concentration
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0051561
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051561_Positive_regulation_of_mitochondrial_calcium_ion_concentration 


id: 39237
description: GO:0051562 Negative regulation of mitochondrial calcium ion concentration
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0051562
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051562_Negative_regulation_of_mitochondrial_calcium_ion_concentration 


id: 39242
description: GO:0051584 Regulation of dopamine uptake involved in synaptic transmission
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0051584
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051584_Regulation_of_dopamine_uptake_involved_in_synaptic_transmission 


id: 39292
description: GO:0051703 Biological process involved in intraspecies interaction between organisms
n: 35
memo: https://amigo.geneontology.org/amigo/term/GO:0051703
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051703_Biological_process_involved_in_intraspecies_interaction_between_organisms 


id: 39303
description: GO:0051770 Positive regulation of nitric-oxide synthase biosynthetic process
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0051770
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051770_Positive_regulation_of_nitric-oxide_synthase_biosynthetic_process 


id: 39304
description: GO:0051771 Negative regulation of nitric-oxide synthase biosynthetic process
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0051771
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051771_Negative_regulation_of_nitric-oxide_synthase_biosynthetic_process 


id: 39338
description: GO:0051896 Regulation of phosphatidylinositol 3-kinase/protein kinase b signal transduction
n: 171
memo: https://amigo.geneontology.org/amigo/term/GO:0051896
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051896_Regulation_of_phosphatidylinositol_3-kinase/protein_kinase_b_signal_transduction 


id: 39339
n: 115
memo: https://amigo.geneontology.org/amigo/term/GO:0051897
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051897_Positive_regulation_of_phosphatidylinositol_3-kinase/protein_kinase_b_signal_transduction 

description:
  GO:0051897 Positive regulation of phosphatidylinositol 3-kinase/protein kinase b signal transduction 


id: 39340
n: 42
memo: https://amigo.geneontology.org/amigo/term/GO:0051898
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051898_Negative_regulation_of_phosphatidylinositol_3-kinase/protein_kinase_b_signal_transduction 

description:
  GO:0051898 Negative regulation of phosphatidylinositol 3-kinase/protein kinase b signal transduction 


id: 39363
description: GO:0051940 Regulation of catecholamine uptake involved in synaptic transmission
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0051940
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051940_Regulation_of_catecholamine_uptake_involved_in_synaptic_transmission 


id: 39364
description: GO:0051941 Regulation of amino acid uptake involved in synaptic transmission
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0051941
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051941_Regulation_of_amino_acid_uptake_involved_in_synaptic_transmission 


id: 39365
description: GO:0051943 Positive regulation of amino acid uptake involved in synaptic transmission
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0051943
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051943_Positive_regulation_of_amino_acid_uptake_involved_in_synaptic_transmission 


id: 39366
description: GO:0051946 Regulation of glutamate uptake involved in transmission of nerve impulse
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0051946
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051946_Regulation_of_glutamate_uptake_involved_in_transmission_of_nerve_impulse 


id: 39367
description: GO:0051951 Positive regulation of glutamate uptake involved in transmission of nerve impulse
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0051951
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051951_Positive_regulation_of_glutamate_uptake_involved_in_transmission_of_nerve_impulse 


id: 39388
description: GO:0051987 Positive regulation of attachment of spindle microtubules to kinetochore
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0051987
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051987_Positive_regulation_of_attachment_of_spindle_microtubules_to_kinetochore 


id: 39389
description: GO:0051988 Regulation of attachment of spindle microtubules to kinetochore
n: 13
memo: https://amigo.geneontology.org/amigo/term/GO:0051988
name:
  GOBP_clfamiliaris_ens_gskb_GO:0051988_Regulation_of_attachment_of_spindle_microtubules_to_kinetochore 


id: 39390
description: GO:0052008 Symbiont-mediated disruption of host cellular anatomical entity
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0052008
name:
  GOBP_clfamiliaris_ens_gskb_GO:0052008_Symbiont-mediated_disruption_of_host_cellular_anatomical_entity 


id: 39487
description: GO:0060054 Positive regulation of epithelial cell proliferation involved in wound healing
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0060054
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060054_Positive_regulation_of_epithelial_cell_proliferation_involved_in_wound_healing 


id: 39491
description: GO:0060058 Positive regulation of apoptotic process involved in mammary gland involution
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060058
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060058_Positive_regulation_of_apoptotic_process_involved_in_mammary_gland_involution 


id: 39533
description: GO:0060143 Positive regulation of syncytium formation by plasma membrane fusion
n: 16
memo: https://amigo.geneontology.org/amigo/term/GO:0060143
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060143_Positive_regulation_of_syncytium_formation_by_plasma_membrane_fusion 


id: 39541
description: GO:0060158 Phospholipase c-activating dopamine receptor signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0060158
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060158_Phospholipase_c-activating_dopamine_receptor_signaling_pathway 


id: 39557
description: GO:0060211 Regulation of nuclear-transcribed mrna poly(a) tail shortening
n: 10
memo: https://amigo.geneontology.org/amigo/term/GO:0060211
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060211_Regulation_of_nuclear-transcribed_mrna_poly(a)_tail_shortening 


id: 39558
description: GO:0060212 Negative regulation of nuclear-transcribed mrna poly(a) tail shortening
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060212
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060212_Negative_regulation_of_nuclear-transcribed_mrna_poly(a)_tail_shortening 


id: 39559
description: GO:0060213 Positive regulation of nuclear-transcribed mrna poly(a) tail shortening
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0060213
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060213_Positive_regulation_of_nuclear-transcribed_mrna_poly(a)_tail_shortening 


id: 39571
description: GO:0060244 Negative regulation of cell proliferation involved in contact inhibition
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060244
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060244_Negative_regulation_of_cell_proliferation_involved_in_contact_inhibition 


id: 39580
description: GO:0060261 Positive regulation of transcription initiation by rna polymerase ii
n: 32
memo: https://amigo.geneontology.org/amigo/term/GO:0060261
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060261_Positive_regulation_of_transcription_initiation_by_rna_polymerase_ii 


id: 39582
description: GO:0060264 Regulation of respiratory burst involved in inflammatory response
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060264
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060264_Regulation_of_respiratory_burst_involved_in_inflammatory_response 


id: 39583
description: GO:0060266 Negative regulation of respiratory burst involved in inflammatory response
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060266
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060266_Negative_regulation_of_respiratory_burst_involved_in_inflammatory_response 


id: 39593
description: GO:0060287 Epithelial cilium movement involved in determination of left/right asymmetry
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0060287
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060287_Epithelial_cilium_movement_involved_in_determination_of_left/right_asymmetry 


id: 39599
description: GO:0060296 Regulation of cilium beat frequency involved in ciliary motility
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0060296
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060296_Regulation_of_cilium_beat_frequency_involved_in_ciliary_motility 


id: 39604
description: GO:0060307 Regulation of ventricular cardiac muscle cell membrane repolarization
n: 17
memo: https://amigo.geneontology.org/amigo/term/GO:0060307
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060307_Regulation_of_ventricular_cardiac_muscle_cell_membrane_repolarization 


id: 39619
description: GO:0060335 Positive regulation of type ii interferon-mediated signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060335
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060335_Positive_regulation_of_type_ii_interferon-mediated_signaling_pathway 


id: 39620
description: GO:0060336 Negative regulation of type ii interferon-mediated signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060336
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060336_Negative_regulation_of_type_ii_interferon-mediated_signaling_pathway 


id: 39623
description: GO:0060339 Negative regulation of type i interferon-mediated signaling pathway
n: 19
memo: https://amigo.geneontology.org/amigo/term/GO:0060339
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060339_Negative_regulation_of_type_i_interferon-mediated_signaling_pathway 


id: 39624
description: GO:0060340 Positive regulation of type i interferon-mediated signaling pathway
n: 16
memo: https://amigo.geneontology.org/amigo/term/GO:0060340
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060340_Positive_regulation_of_type_i_interferon-mediated_signaling_pathway 


id: 39632
description: GO:0060351 Cartilage development involved in endochondral bone morphogenesis
n: 30
memo: https://amigo.geneontology.org/amigo/term/GO:0060351
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060351_Cartilage_development_involved_in_endochondral_bone_morphogenesis 


id: 39638
description: GO:0060368 Regulation of fc receptor mediated stimulatory signaling pathway
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0060368
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060368_Regulation_of_fc_receptor_mediated_stimulatory_signaling_pathway 


id: 39639
description: GO:0060369 Positive regulation of fc receptor mediated stimulatory signaling pathway
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060369
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060369_Positive_regulation_of_fc_receptor_mediated_stimulatory_signaling_pathway 


id: 39640
description: GO:0060371 Regulation of atrial cardiac muscle cell membrane depolarization
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0060371
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060371_Regulation_of_atrial_cardiac_muscle_cell_membrane_depolarization 


id: 39641
description: GO:0060372 Regulation of atrial cardiac muscle cell membrane repolarization
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060372
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060372_Regulation_of_atrial_cardiac_muscle_cell_membrane_repolarization 


id: 39642
description: GO:0060373 Regulation of ventricular cardiac muscle cell membrane depolarization
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0060373
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060373_Regulation_of_ventricular_cardiac_muscle_cell_membrane_depolarization 


id: 39657
description: GO:0060400 Negative regulation of growth hormone receptor signaling pathway
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060400
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060400_Negative_regulation_of_growth_hormone_receptor_signaling_pathway 


id: 39689
description: GO:0060448 Dichotomous subdivision of terminal units involved in lung branching
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060448
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060448_Dichotomous_subdivision_of_terminal_units_involved_in_lung_branching 


id: 39714
description: GO:0060501 Positive regulation of epithelial cell proliferation involved in lung morphogenesis
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060501
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060501_Positive_regulation_of_epithelial_cell_proliferation_involved_in_lung_morphogenesis 


id: 39724
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0060527
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060527_Prostate_epithelial_cord_arborization_involved_in_prostate_glandular_acinus_morphogenesis 

description:
  GO:0060527 Prostate epithelial cord arborization involved in prostate glandular acinus morphogenesis 


id: 39742
description: GO:0060566 Positive regulation of termination of dna-templated transcription
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060566
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060566_Positive_regulation_of_termination_of_dna-templated_transcription 


id: 39743
description: GO:0060567 Negative regulation of termination of dna-templated transcription
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060567
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060567_Negative_regulation_of_termination_of_dna-templated_transcription 


id: 39773
description: GO:0060633 Negative regulation of transcription initiation by rna polymerase ii
n: 7
memo: https://amigo.geneontology.org/amigo/term/GO:0060633
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060633_Negative_regulation_of_transcription_initiation_by_rna_polymerase_ii 


id: 39778
description: GO:0060664 Epithelial cell proliferation involved in salivary gland morphogenesis
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060664
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060664_Epithelial_cell_proliferation_involved_in_salivary_gland_morphogenesis 


id: 39779
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060665
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060665_Regulation_of_branching_involved_in_salivary_gland_morphogenesis_by_mesenchymal-epithelial_signaling 

description:
  GO:0060665 Regulation of branching involved in salivary gland morphogenesis by mesenchymal-epithelial signaling 


id: 39780
description: GO:0060666 Dichotomous subdivision of terminal units involved in salivary gland branching
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060666
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060666_Dichotomous_subdivision_of_terminal_units_involved_in_salivary_gland_branching 


id: 39783
description: GO:0060671 Epithelial cell differentiation involved in embryonic placenta development
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060671
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060671_Epithelial_cell_differentiation_involved_in_embryonic_placenta_development 


id: 39784
description: GO:0060672 Epithelial cell morphogenesis involved in placental branching
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060672
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060672_Epithelial_cell_morphogenesis_involved_in_placental_branching 


id: 39793
description: GO:0060687 Regulation of branching involved in prostate gland morphogenesis
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0060687
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060687_Regulation_of_branching_involved_in_prostate_gland_morphogenesis 


id: 39796
description: GO:0060693 Regulation of branching involved in salivary gland morphogenesis
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0060693
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060693_Regulation_of_branching_involved_in_salivary_gland_morphogenesis 


id: 39799
description: GO:0060706 Cell differentiation involved in embryonic placenta development
n: 20
memo: https://amigo.geneontology.org/amigo/term/GO:0060706
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060706_Cell_differentiation_involved_in_embryonic_placenta_development 


id: 39810
description: GO:0060732 Positive regulation of inositol phosphate biosynthetic process
n: 6
memo: https://amigo.geneontology.org/amigo/term/GO:0060732
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060732_Positive_regulation_of_inositol_phosphate_biosynthetic_process 


id: 39814
description: GO:0060742 Epithelial cell differentiation involved in prostate gland development
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0060742
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060742_Epithelial_cell_differentiation_involved_in_prostate_gland_development 


id: 39815
description: GO:0060743 Epithelial cell maturation involved in prostate gland development
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060743
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060743_Epithelial_cell_maturation_involved_in_prostate_gland_development 


id: 39819
description: GO:0060748 Tertiary branching involved in mammary gland duct morphogenesis
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060748
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060748_Tertiary_branching_involved_in_mammary_gland_duct_morphogenesis 


id: 39821
description: GO:0060750 Epithelial cell proliferation involved in mammary gland duct elongation
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0060750
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060750_Epithelial_cell_proliferation_involved_in_mammary_gland_duct_elongation 


id: 39829
description: GO:0060762 Regulation of branching involved in mammary gland duct morphogenesis
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060762
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060762_Regulation_of_branching_involved_in_mammary_gland_duct_morphogenesis 


id: 39834
description: GO:0060767 Epithelial cell proliferation involved in prostate gland development
n: 9
memo: https://amigo.geneontology.org/amigo/term/GO:0060767
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060767_Epithelial_cell_proliferation_involved_in_prostate_gland_development 


id: 39835
description: GO:0060768 Regulation of epithelial cell proliferation involved in prostate gland development
n: 8
memo: https://amigo.geneontology.org/amigo/term/GO:0060768
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060768_Regulation_of_epithelial_cell_proliferation_involved_in_prostate_gland_development 


id: 39836
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060769
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060769_Positive_regulation_of_epithelial_cell_proliferation_involved_in_prostate_gland_development 

description:
  GO:0060769 Positive regulation of epithelial cell proliferation involved in prostate gland development 


id: 39837
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0060770
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060770_Negative_regulation_of_epithelial_cell_proliferation_involved_in_prostate_gland_development 

description:
  GO:0060770 Negative regulation of epithelial cell proliferation involved in prostate gland development 


id: 39840
description: GO:0060795 Cell fate commitment involved in formation of primary germ layer
n: 23
memo: https://amigo.geneontology.org/amigo/term/GO:0060795
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060795_Cell_fate_commitment_involved_in_formation_of_primary_germ_layer 


id: 39841
description: GO:0060800 Regulation of cell differentiation involved in embryonic placenta development
n: 4
memo: https://amigo.geneontology.org/amigo/term/GO:0060800
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060800_Regulation_of_cell_differentiation_involved_in_embryonic_placenta_development 


id: 39842
description: GO:0060809 Mesodermal to mesenchymal transition involved in gastrulation
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0060809
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060809_Mesodermal_to_mesenchymal_transition_involved_in_gastrulation 


id: 39846
description: GO:0060831 Smoothened signaling pathway involved in dorsal/ventral neural tube patterning
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0060831
name:
  GOBP_clfamiliaris_ens_gskb_GO:0060831_Smoothened_signaling_pathway_involved_in_dorsal/ventral_neural_tube_patterning 


id: 39915
description: GO:0061030 Epithelial cell differentiation involved in mammary gland alveolus development
n: 3
memo: https://amigo.geneontology.org/amigo/term/GO:0061030
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061030_Epithelial_cell_differentiation_involved_in_mammary_gland_alveolus_development 


id: 39929
description: GO:0061047 Positive regulation of branching involved in lung morphogenesis
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0061047
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061047_Positive_regulation_of_branching_involved_in_lung_morphogenesis 


id: 39931
description: GO:0061050 Regulation of cell growth involved in cardiac muscle cell development
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0061050
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061050_Regulation_of_cell_growth_involved_in_cardiac_muscle_cell_development 


id: 39932
description: GO:0061051 Positive regulation of cell growth involved in cardiac muscle cell development
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0061051
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061051_Positive_regulation_of_cell_growth_involved_in_cardiac_muscle_cell_development 


id: 39933
description: GO:0061052 Negative regulation of cell growth involved in cardiac muscle cell development
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0061052
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061052_Negative_regulation_of_cell_growth_involved_in_cardiac_muscle_cell_development 


id: 39943
n: 21
memo: https://amigo.geneontology.org/amigo/term/GO:0061081
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061081_Positive_regulation_of_myeloid_leukocyte_cytokine_production_involved_in_immune_response 

description:
  GO:0061081 Positive regulation of myeloid leukocyte cytokine production involved in immune response 


id: 39966
description: GO:0061159 Establishment of bipolar cell polarity involved in cell morphogenesis
n: 2
memo: https://amigo.geneontology.org/amigo/term/GO:0061159
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061159_Establishment_of_bipolar_cell_polarity_involved_in_cell_morphogenesis 


id: 39969
description: GO:0061178 Regulation of insulin secretion involved in cellular response to glucose stimulus
n: 36
memo: https://amigo.geneontology.org/amigo/term/GO:0061178
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061178_Regulation_of_insulin_secretion_involved_in_cellular_response_to_glucose_stimulus 


id: 39970
n: 5
memo: https://amigo.geneontology.org/amigo/term/GO:0061179
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061179_Negative_regulation_of_insulin_secretion_involved_in_cellular_response_to_glucose_stimulus 

description:
  GO:0061179 Negative regulation of insulin secretion involved in cellular response to glucose stimulus 


id: 39990
description: GO:0061307 Cardiac neural crest cell differentiation involved in heart development
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0061307
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061307_Cardiac_neural_crest_cell_differentiation_involved_in_heart_development 


id: 39991
description: GO:0061308 Cardiac neural crest cell development involved in heart development
n: 12
memo: https://amigo.geneontology.org/amigo/term/GO:0061308
name:
  GOBP_clfamiliaris_ens_gskb_GO:0061308_Cardiac_neural_crest_cell_development_involved_in_heart_development 


