Name

Molybdenum cofactor deficiency, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Molybdenum cofactor deficiency, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Molybdenum cofactor deficiency, complementation group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Molybdenum cofactor deficiency, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Molybdenum cofactor deficiency, complementation group B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Molybdenum cofactor deficiency, complementation group B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Molybdenum cofactor deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Molybdenum cofactor deficiency from the curated CTD Gene-Disease Associations dataset.

molybdenum cofactor deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the molybdenum cofactor deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

molybdenum cofactor deficiency b Gene Set

From OMIM Gene-Disease Associations

genes associated with the molybdenum cofactor deficiency b phenotype from the curated OMIM Gene-Disease Associations dataset.

molybdenum cofactor deficiency c Gene Set

From OMIM Gene-Disease Associations

genes associated with the molybdenum cofactor deficiency c phenotype from the curated OMIM Gene-Disease Associations dataset.

molybdenum cofactor deficiency a Gene Set

From OMIM Gene-Disease Associations

genes associated with the molybdenum cofactor deficiency a phenotype from the curated OMIM Gene-Disease Associations dataset.

molybdenum incorporation into molybdenum-molybdopterin complex Gene Set

From GO Biological Process Annotations

genes participating in the molybdenum incorporation into molybdenum-molybdopterin complex biological process from the curated GO Biological Process Annotations dataset.

thio-molybdenum cofactor biosynthesis Gene Set

From HumanCyc Pathways

proteins participating in the thio-molybdenum cofactor biosynthesis pathway from the HumanCyc Pathways dataset.

molybdenum cofactor biosynthesis Gene Set

From HumanCyc Pathways

proteins participating in the molybdenum cofactor biosynthesis pathway from the HumanCyc Pathways dataset.

Molybdenum cofactor biosynthesis C, bacterial-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor biosynthesis C, bacterial-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor sulfurase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor sulfurase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor sulfurase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor sulfurase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor synthesis C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor synthesis C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor biosynthesis C Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor biosynthesis C protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor biosynthesis, MoeB Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor biosynthesis, MoeB protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor biosynthesis protein A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor biosynthesis protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor biosynthesis, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdenum cofactor biosynthesis, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdenum cofactor biosynthesis Gene Set

From Reactome Pathways

proteins participating in the Molybdenum cofactor biosynthesis pathway from the Reactome Pathways dataset.

mhc class ii deficiency, complementation group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the mhc class ii deficiency, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset.

Fanconi anemia, complementation group O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group D2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group D2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP C from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP E from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP F from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group J from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group B from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group N Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group N from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP D2 from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group I from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP O Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP O from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group D1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group D1 from the curated CTD Gene-Disease Associations dataset.

fanconi anemia, complementation group p Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group p phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group q Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group q phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group i Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group i phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group j Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group j phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group l Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group l phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group m Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group m phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group n Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group n phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group o Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group o phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group f Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group f phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group g Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group g phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group d1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group d1 phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group d2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group d2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, complementation group b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, complementation group b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma Pigmentosum, Complementation Group C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group C from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group B from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group E from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group D from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group G from the curated CTD Gene-Disease Associations dataset.

Xeroderma Pigmentosum, Complementation Group F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group F from the curated CTD Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset.

trichothiodystrophy, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichothiodystrophy, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

Heparin Cofactor II Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heparin Cofactor II Deficiency from the curated CTD Gene-Disease Associations dataset.

thrombophilia due to heparin cofactor ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Molybdenum Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Molybdenum from the curated CTD Gene-Chemical Interactions dataset.

molybdenum chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical molybdenum chloride from the curated CTD Gene-Chemical Interactions dataset.

molybdenum trioxide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical molybdenum trioxide from the curated CTD Gene-Chemical Interactions dataset.

(Molybdopterin-S,S)-Dioxo-Thio-Molybdenum(V) Gene Set

From DrugBank Drug Targets

interacting proteins for the (Molybdopterin-S,S)-Dioxo-Thio-Molybdenum(V) drug from the curated DrugBank Drug Targets dataset.

molybdenum Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term molybdenum in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

molybdenum ion binding Gene Set

From GO Molecular Function Annotations

genes performing the molybdenum ion binding molecular function from the curated GO Molecular Function Annotations dataset.

Molybdenum Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Molybdenum metabolite from the curated HMDB Metabolites of Enzymes dataset.

phospholipase a2, group iv a, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the phospholipase a2, group iv a, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

cofactor transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cofactor transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii transcription cofactor activity Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii transcription cofactor activity molecular function from the curated GO Molecular Function Annotations dataset.

transcription cofactor activity Gene Set

From GO Molecular Function Annotations

genes performing the transcription cofactor activity molecular function from the curated GO Molecular Function Annotations dataset.

quinone cofactor methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the quinone cofactor methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

mo-molybdopterin cofactor sulfurase activity Gene Set

From GO Molecular Function Annotations

genes performing the mo-molybdopterin cofactor sulfurase activity molecular function from the curated GO Molecular Function Annotations dataset.

abnormal vitamin or vitamin cofactor metabolism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vitamin or vitamin cofactor metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Formation of the active cofactor, UDP-glucuronate Gene Set

From Reactome Pathways

proteins participating in the Formation of the active cofactor, UDP-glucuronate pathway from the Reactome Pathways dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

homocystinuria-megaloblastic anemia, cblg complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria-megaloblastic anemia, cblg complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

negative cofactor 2 complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the negative cofactor 2 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cofactor Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cofactor in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cofactor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the cofactor catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of cofactor metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cofactor metabolic process biological process from the curated GO Biological Process Annotations dataset.

molybdopterin cofactor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the molybdopterin cofactor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

mo-molybdopterin cofactor metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mo-molybdopterin cofactor metabolic process biological process from the curated GO Biological Process Annotations dataset.

chaperone cofactor-dependent protein refolding Gene Set

From GO Biological Process Annotations

genes participating in the chaperone cofactor-dependent protein refolding biological process from the curated GO Biological Process Annotations dataset.

molybdopterin cofactor metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the molybdopterin cofactor metabolic process biological process from the curated GO Biological Process Annotations dataset.

peptidyl-pyrromethane cofactor linkage Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-pyrromethane cofactor linkage biological process from the curated GO Biological Process Annotations dataset.

cofactor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the cofactor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

protein-cofactor linkage Gene Set

From GO Biological Process Annotations

genes participating in the protein-cofactor linkage biological process from the curated GO Biological Process Annotations dataset.

cofactor transport Gene Set

From GO Biological Process Annotations

genes participating in the cofactor transport biological process from the curated GO Biological Process Annotations dataset.

cofactor metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the cofactor metabolic process biological process from the curated GO Biological Process Annotations dataset.

mo-molybdopterin cofactor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the mo-molybdopterin cofactor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

chaperone mediated protein folding requiring cofactor Gene Set

From GO Biological Process Annotations

genes participating in the chaperone mediated protein folding requiring cofactor biological process from the curated GO Biological Process Annotations dataset.

transcription cofactor binding Gene Set

From GO Molecular Function Annotations

genes performing the transcription cofactor binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii transcription cofactor binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii transcription cofactor binding molecular function from the curated GO Molecular Function Annotations dataset.

molybdopterin cofactor binding Gene Set

From GO Molecular Function Annotations

genes performing the molybdopterin cofactor binding molecular function from the curated GO Molecular Function Annotations dataset.

cofactor binding Gene Set

From GO Molecular Function Annotations

genes performing the cofactor binding molecular function from the curated GO Molecular Function Annotations dataset.

Molybdopterin cofactor biosynthesis C (MoaC) domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdopterin cofactor biosynthesis C (MoaC) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Moybdenum cofactor oxidoreductase, dimerisation Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Moybdenum cofactor oxidoreductase, dimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.

C-CAP/cofactor C-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the C-CAP/cofactor C-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tubulin binding cofactor C-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tubulin binding cofactor C-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription cofactor vestigial-like protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription cofactor vestigial-like protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Membrane cofactor protein CD46 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane cofactor protein CD46 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Porphobilinogen deaminase, dipyrromethane cofactor binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Porphobilinogen deaminase, dipyrromethane cofactor binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cofactor of BRCA1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cofactor of BRCA1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Na(+)/H(+) exchange regulatory cofactor NHE-RF Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Na(+)/H(+) exchange regulatory cofactor NHE-RF protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tubulin binding cofactor A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tubulin binding cofactor A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

complementation Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term complementation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choline deficiency; dna damage; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Neuraminidase deficiency with beta-galactosidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.

eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein c deficiency; protein s deficiency; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.

anterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior digastric muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Dopaminergic A13 group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Dopaminergic A13 group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antigen in Scianna blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antigen in Scianna blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WRIGHT ANTIGEN Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WRIGHT ANTIGEN phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monoisopropyl Ester Phosphonic Acid Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Monoisopropyl Ester Phosphonic Acid Group drug from the curated DrugBank Drug Targets dataset.

Methylphosphonic Acid Ester Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Methylphosphonic Acid Ester Group drug from the curated DrugBank Drug Targets dataset.

i/d ace gene polymorphism and abo blood group system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease i/d ace gene polymorphism and abo blood group system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

quaternary ammonium group transport Gene Set

From GO Biological Process Annotations

genes participating in the quaternary ammonium group transport biological process from the curated GO Biological Process Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

phosphotransferase activity, phosphate group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, phosphate group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

quaternary ammonium group transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the quaternary ammonium group transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

steroid dehydrogenase activity, acting on the ch-oh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the steroid dehydrogenase activity, acting on the ch-oh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a heme group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a heme group of donors molecular function from the curated GO Molecular Function Annotations dataset.

quaternary ammonium group binding Gene Set

From GO Molecular Function Annotations

genes performing the quaternary ammonium group binding molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

phosphotransferase activity, nitrogenous group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on ch-oh group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on ch-oh group of donors molecular function from the curated GO Molecular Function Annotations dataset.

group ii metabotropic glutamate receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the group ii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors molecular function from the curated GO Molecular Function Annotations dataset.

steroid dehydrogenase activity, acting on the ch-ch group of donors Gene Set

From GO Molecular Function Annotations

genes performing the steroid dehydrogenase activity, acting on the ch-ch group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

group iii metabotropic glutamate receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the group iii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

phosphotransferase activity, carboxyl group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, carboxyl group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

phosphotransferase activity, alcohol group as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-nh group of donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-nh group of donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations dataset.

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

G-protein alpha subunit, group I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G-protein alpha subunit, group S Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group S protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G-protein alpha subunit, group Q Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group Q protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anaemia group C protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anaemia group C protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G-protein alpha subunit, group 12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G-protein alpha subunit, group 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anemia group I protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anemia group I protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi Anaemia group E protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi Anaemia group E protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alanine racemase/group IV decarboxylase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alanine racemase/group IV decarboxylase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anaemia group A protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anaemia group A protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

[blood group, abo system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, abo system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, auberger system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, auberger system] phenotype from the curated OMIM Gene-Disease Associations dataset.

phosphotransferases-alcohol-group-acceptor Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term phosphotransferases-alcohol-group-acceptor in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

gigantocellular group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gigantocellular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central medullary reticular group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

rostral group of intralaminar nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

caudal group of intralaminar nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in caudal group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

rostral group of intralaminar nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral medullary reticular group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

caudal group of intralaminar nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in caudal group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, left, ventral division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, left, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

gigantocellular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in gigantocellular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, right, ventral division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, right, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cortico-medial group, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cortico-medial group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral medullary reticular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cortico-medial group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cortico-medial group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, left, dorsal division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, left, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

posterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral group of nuclei, right, dorsal division Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral group of nuclei, right, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

medial group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

central medullary reticular group, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Geniculate group, ventral thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Geniculate group, ventral thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medial group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medial group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

A4 noradrenergic cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in A4 noradrenergic cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

temporal muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in temporal muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Geniculate group, dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Geniculate group, dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Ventral group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Ventral group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r5 part of A5 noradrenergic cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r5 part of A5 noradrenergic cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

pterigoid muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in pterigoid muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

temporotympanic muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in temporotympanic muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Midline group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Midline group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

rostral ventral respiratory cell group Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral ventral respiratory cell group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

central nuclear group Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in central nuclear group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Blood group, john milton hagen system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, john milton hagen system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WALDNER TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WALDNER TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cromer blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cromer blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Radin blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Radin blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, junior system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, junior system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, gerbich system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, gerbich system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--OK Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--OK phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Langereis blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Langereis blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--FROESE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--FROESE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--LUTHERAN INHIBITOR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--LUTHERAN INHIBITOR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, dombrock system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, dombrock system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Xeroderma pigmentosum, group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Xeroderma pigmentosum, group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

blood group incompatibility Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood group incompatibility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Diisopropylphosphono Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Diisopropylphosphono Group drug from the curated DrugBank Drug Targets dataset.

4-Methylpiperazin-1-Yl Carbonyl Group Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-Methylpiperazin-1-Yl Carbonyl Group drug from the curated DrugBank Drug Targets dataset.

(1S)-MENTHYL HEXYL PHOSPHONATE GROUP Gene Set

From DrugBank Drug Targets

interacting proteins for the (1S)-MENTHYL HEXYL PHOSPHONATE GROUP drug from the curated DrugBank Drug Targets dataset.

(1R)-MENTHYL HEXYL PHOSPHONATE GROUP Gene Set

From DrugBank Drug Targets

interacting proteins for the (1R)-MENTHYL HEXYL PHOSPHONATE GROUP drug from the curated DrugBank Drug Targets dataset.

Pyruvoyl Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Pyruvoyl Group drug from the curated DrugBank Drug Targets dataset.

Diethylphosphono Group Gene Set

From DrugBank Drug Targets

interacting proteins for the Diethylphosphono Group drug from the curated DrugBank Drug Targets dataset.

2-Bromoacetyl Group Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-Bromoacetyl Group drug from the curated DrugBank Drug Targets dataset.

blood group incompatibility; rh isoimmunization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood group incompatibility; rh isoimmunization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; blood group incompatibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; blood group incompatibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

group Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term group in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

prosthetic group metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the prosthetic group metabolic process biological process from the curated GO Biological Process Annotations dataset.

prosthetic group binding Gene Set

From GO Molecular Function Annotations

genes performing the prosthetic group binding molecular function from the curated GO Molecular Function Annotations dataset.

group E 1682-2106 [PMID:16118363] Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the group E 1682-2106 [PMID:16118363] ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Psychotherapy, Group Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Psychotherapy, Group phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Group Incompatibility Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Group Incompatibility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cytochrome P450, E-class, group I, CYP1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2D-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2D-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pre-SET zinc-binding sub-group Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pre-SET zinc-binding sub-group protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2J-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2J-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group box domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group IV Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group IV protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Xeroderma pigmentosum group D protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Xeroderma pigmentosum group D protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Blood group Rhesus C/E/D polypeptide Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Blood group Rhesus C/E/D polypeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2B-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2B-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group, HMG-I/HMG-Y Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group, HMG-I/HMG-Y protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phospholipase A2, group XII secretory Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phospholipase A2, group XII secretory protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group nucleosome-binding domain-containing family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group nucleosome-binding domain-containing family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2A-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2A-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kell blood group glycoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kell blood group glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bacterial Ig-like, group 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bacterial Ig-like, group 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, E-class, group I, CYP2E-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, E-class, group I, CYP2E-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group box domain 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group box domain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

[blood group, swann] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, swann] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rodgers] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rodgers] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, colton] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, colton] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, knops system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, knops system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[junior blood group system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [junior blood group system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, raph] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, raph] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group gil] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group gil] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, dombrock] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, dombrock] phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group g/cockayne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group g/cockayne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, waldner] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, waldner] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, scianna system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, scianna system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, mn] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, mn] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, xg system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, xg system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lutheran system] phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group b phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group c phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group a phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group f Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group f phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group g Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group g phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group d phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ok] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ok] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, indian system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, indian system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, froese] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, froese] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, landsteiner-wiener] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, landsteiner-wiener] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rhesus] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rhesus] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, globoside system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, globoside system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran null] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lutheran null] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, kell] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, kell] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, radin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, radin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, kidd] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, kidd] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, yt system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, yt system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p(k) phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p(k) phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

blood group--lutheran inhibitor Gene Set

From OMIM Gene-Disease Associations

genes associated with the blood group--lutheran inhibitor phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, vel system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, vel system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ss] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ss] phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, group e, ddb-negative subtype Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, group e, ddb-negative subtype phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, stoltzfus system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, stoltzfus system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lewis] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, lewis] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, diego] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, diego] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, ii] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, ii] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, langereis system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, langereis system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, gerbich] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, gerbich] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, wright] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, wright] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group cromer] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group cromer] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, john-milton-hagen system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, john-milton-hagen system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, p1pk system, p(2) phenotype] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, p1pk system, p(2) phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, duffy system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, duffy system] phenotype from the curated OMIM Gene-Disease Associations dataset.

Metabotropic glutamate receptor group I pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group I pathway pathway from the PANTHER Pathways dataset.

Metabotropic glutamate receptor group III pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group III pathway pathway from the PANTHER Pathways dataset.

Metabotropic glutamate receptor group II pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group II pathway pathway from the PANTHER Pathways dataset.

Human immunodeficiency virus type 1 group M subtype B (isolate MN) Gene Set

From Virus MINT Protein-Virus Interactions

interacting proteins for the virus Human immunodeficiency virus type 1 group M subtype B (isolate MN) from the Virus MINT Protein-Virus Interactions dataset.

anemia, iron deficiency; anemia of chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron deficiency; anemia of chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; glucosephosphate dehydrogenase deficiency; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; glucosephosphate dehydrogenase deficiency; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Endplate acetylcholinesterase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Endplate acetylcholinesterase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methionine adenosyltransferase deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

N-terminal acetyltransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the N-terminal acetyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acyl-CoA dehydrogenase family, member 9, deficiency of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acyl-CoA dehydrogenase family, member 9, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phosphoserine aminotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phosphoserine aminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carnitine acylcarnitine translocase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carnitine acylcarnitine translocase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Succinyl-CoA acetoacetate transferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Succinyl-CoA acetoacetate transferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HNSHA due to aldolase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-activating factor acetylhydrolase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-activating factor acetylhydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucocorticoid deficiency with achalasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucocorticoid deficiency with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant isolated somatotropin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anhidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Plasminogen activator inhibitor type 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Plasminogen activator inhibitor type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenine phosphoribosyltransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenine phosphoribosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

N-acetylaspartate deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the N-acetylaspartate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylosuccinate lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aromatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aromatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia with vitamin E deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ACTH deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ACTH deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antithrombin III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth hormone deficiency with pituitary anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth hormone deficiency with pituitary anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase lipoic acid synthetase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arginase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arginase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha-fetoprotein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha-fetoprotein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia due to adenosine kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukocyte adhesion deficiency type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukocyte adhesion deficiency type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anaphylotoxin inactivator deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anaphylotoxin inactivator deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocyte amp deaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocyte amp deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Apolipoprotein a-i deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Apolipoprotein a-i deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glut1 deficiency syndrome 1, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-aminobutyric acid transaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-aminobutyric acid transaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Very long chain acyl-CoA dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukocyte adhesion deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukocyte adhesion deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arginine:glycine amidinotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arginine:glycine amidinotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methionine adenosyltransferase deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscle AMP deaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscle AMP deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase E1-alpha deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase E1-alpha deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ornithine aminotransferase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ornithine aminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sphingolipid activator protein 1 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sphingolipid activator protein 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lysosomal acid lipase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lysosomal acid lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of alpha-mannosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of alpha-mannosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Argininosuccinate lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Argininosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked agammaglobulinemia with growth hormone deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked agammaglobulinemia with growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of acetyl-CoA acetyltransferase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of acetyl-CoA acetyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acid-labile subunit deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of aromatic-L-amino-acid decarboxylase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of aromatic-L-amino-acid decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asparagine synthetase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asparagine synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylate kinase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of factor V and factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of sialidase AND beta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia, Iron-Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Iron-Deficiency from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Leukocyte Adhesion Deficiency, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukocyte Adhesion Deficiency, Type III from the curated CTD Gene-Disease Associations dataset.

Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.

Aniridia cerebellar ataxia mental deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Adenosine monophosphate deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenosine monophosphate deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

alpha 1-Antitrypsin Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease alpha 1-Antitrypsin Deficiency from the curated CTD Gene-Disease Associations dataset.

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Lecithin Acyltransferase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lecithin Acyltransferase Deficiency from the curated CTD Gene-Disease Associations dataset.

Interleukin 2 Receptor, Alpha, Deficiency of Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Interleukin 2 Receptor, Alpha, Deficiency of from the curated CTD Gene-Disease Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.

Folic Acid Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Folic Acid Deficiency from the curated CTD Gene-Disease Associations dataset.

Lysosomal acid lipase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lysosomal acid lipase deficiency from the curated CTD Gene-Disease Associations dataset.

Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.

Carnitine-Acylcarnitine Translocase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carnitine-Acylcarnitine Translocase Deficiency from the curated CTD Gene-Disease Associations dataset.

Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Factor 8 deficiency, acquired Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Factor 8 deficiency, acquired from the curated CTD Gene-Disease Associations dataset.

Adenylosuccinate lyase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylosuccinate lyase deficiency from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Severe combined immunodeficiency due to adenosine deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.

Plasminogen Activator Inhibitor-1 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Plasminogen Activator Inhibitor-1 Deficiency from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Ataxia with vitamin E deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia with vitamin E deficiency from the curated CTD Gene-Disease Associations dataset.

Aromatic amino acid decarboxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aromatic amino acid decarboxylase deficiency from the curated CTD Gene-Disease Associations dataset.

FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset.

N-acetyl glutamate synthetase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease N-acetyl glutamate synthetase deficiency from the curated CTD Gene-Disease Associations dataset.

Aminoacylase 1 deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aminoacylase 1 deficiency from the curated CTD Gene-Disease Associations dataset.

Antithrombin III Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Antithrombin III Deficiency from the curated CTD Gene-Disease Associations dataset.

FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.

Arginine:Glycine Amidinotransferase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arginine:Glycine Amidinotransferase Deficiency from the curated CTD Gene-Disease Associations dataset.

Methionine Adenosyltransferase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methionine Adenosyltransferase Deficiency from the curated CTD Gene-Disease Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

Leukocyte adhesion deficiency type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukocyte adhesion deficiency type 1 from the curated CTD Gene-Disease Associations dataset.

ACTH Deficiency, Isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ACTH Deficiency, Isolated from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

Iron-Refractory Iron Deficiency Anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset.

Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Peroxisomal ACYL-COA oxidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peroxisomal ACYL-COA oxidase deficiency from the curated CTD Gene-Disease Associations dataset.

Endplate Acetylcholinesterase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Endplate Acetylcholinesterase Deficiency from the curated CTD Gene-Disease Associations dataset.

NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Alpha-ketoglutarate dehydrogenase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha-ketoglutarate dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.

Leukocyte-Adhesion Deficiency Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukocyte-Adhesion Deficiency Syndrome from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Medium chain acyl CoA dehydrogenase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Medium chain acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.

Familial apoceruloplasmin deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.

MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Short chain Acyl CoA dehydrogenase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.

Gamma aminobutyric acid transaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma aminobutyric acid transaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Aromatase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aromatase deficiency from the curated CTD Gene-Disease Associations dataset.

Phosphoserine Aminotransferase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Phosphoserine Aminotransferase Deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease alpha 1-antitrypsin deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

agat deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease agat deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

adenosine deaminase deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease adenosine deaminase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

antithrombin iii deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease antithrombin iii deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

iron deficiency anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease iron deficiency anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

leukocyte-adhesion deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease leukocyte-adhesion deficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

folic acid deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease folic acid deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

leukocyte adhesion deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease leukocyte adhesion deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adenosine deaminase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adenosine deaminase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

antithrombin iii deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease antithrombin iii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

iron deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease iron deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

immunoglobulin alpha deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease immunoglobulin alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

artemis deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease artemis deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

agat deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease agat deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

interleukin-7 receptor alpha deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease interleukin-7 receptor alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pyridoxine deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pyridoxine deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

recombinase activating gene 1 deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease recombinase activating gene 1 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

alpha 1-antitrypsin deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease alpha 1-antitrypsin deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

protein-deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease protein-deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ahg deficiency disease; hemophilia a; hemorrhage; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hemorrhage; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; lung neoplasms; neoplasm of lung ; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; lung neoplasms; neoplasm of lung ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adenomatous polyps; colonic polyps; colorectal neoplasms; hyperplasia; magnesium deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adenomatous polyps; colonic polyps; colorectal neoplasms; hyperplasia; magnesium deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; wegener granulomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; fibrosis; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; colorectal neoplasms; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; colorectal neoplasms; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

end-plate acetylcholinesterase deficiency (type ic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease end-plate acetylcholinesterase deficiency (type ic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophic cardiomyopathy and cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophic cardiomyopathy and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leigh syndrome and cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leigh syndrome and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

medium-chain acyl-coa dehydrogenase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease medium-chain acyl-coa dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha(1) antitrypsin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha(1) antitrypsin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive; pulmonary emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

medium-chain acyl-coa dehydrogenase (mcad) deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease medium-chain acyl-coa dehydrogenase (mcad) deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sickle cell anemia; g6pd deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia; g6pd deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acid lipase deficiency and cholesterol ester storage disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acid lipase deficiency and cholesterol ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; lung diseases, obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; lung diseases, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; liver failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; liver failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; cerebral infarction; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; cerebral infarction; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; carcinoma, hepatocellular; hemophilia a; hemophilia b; hepatitis c; lcc - liver cell carcinoma; liver neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; carcinoma, hepatocellular; hemophilia a; hemophilia b; hepatitis c; lcc - liver cell carcinoma; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hepatitis c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; iga deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; folic acid deficiency; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; folic acid deficiency; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin indicate a single origin for deficiency allele pi z Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin indicate a single origin for deficiency allele pi z in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ascorbic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ascorbic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alphal-antitrypsin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alphal-antitrypsin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; folic acid deficiency; gastrointestinal neoplasms; oesophageal neoplasm Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; folic acid deficiency; gastrointestinal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; coronary thrombosis; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; coronary thrombosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; arthritis; hemophilia a; synovitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; arthritis; hemophilia a; synovitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hemophilia b; hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hemophilia b; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acyl-coa dehydrogenase (scad) deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acyl-coa dehydrogenase (scad) deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; liver diseases; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; liver diseases; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum alpha 1-antitrypsin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum alpha 1-antitrypsin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; emphysema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; emphysema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

methionine adenosyltransferase i/iii deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease methionine adenosyltransferase i/iii deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; occupational diseases; smoke inhalation injury Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; occupational diseases; smoke inhalation injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; folic acid deficiency; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; folic acid deficiency; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

iga deficiency and common variable immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease iga deficiency and common variable immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukocyte adhesion deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukocyte adhesion deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; polycythemia vera Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; leukemia, lymphoid; lymphoblastic leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; leukemia, lymphoid; lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; avitaminosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; avitaminosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

iron deficiency anemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease iron deficiency anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

immunoglobulin alpha deficiency Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease immunoglobulin alpha deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

iron deficiency anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the iron deficiency anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

specific antibody deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the specific antibody deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenocorticotropic hormone deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenocorticotropic hormone deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

factor x activation deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the factor x activation deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

specific anti-polysaccharide antibody deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the specific anti-polysaccharide antibody deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

deficiency or absence of cytochrome b(-245) Gene Set

From HPO Gene-Disease Associations

genes associated with the deficiency or absence of cytochrome b(-245) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aldehyde oxidase deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the aldehyde oxidase deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

deficiency of n-acetylglucosamine-1-phosphotransferase Gene Set

From HPO Gene-Disease Associations

genes associated with the deficiency of n-acetylglucosamine-1-phosphotransferase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Anemia, Iron-Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Iron-Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Antithrombin III Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Antithrombin III Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

alpha 1-Antitrypsin Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the alpha 1-Antitrypsin Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lecithin Acyltransferase Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lecithin Acyltransferase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Folic Acid Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Folic Acid Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ascorbic Acid Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ascorbic Acid Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-1-antichymotrypsin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-1-antichymotrypsin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex (atp synthase) deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex (atp synthase) deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

pyruvate dehydrogenase lipoic acid synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

aminoacylase 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aminoacylase 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to phosphofructokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

apolipoprotein a-ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the apolipoprotein a-ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

l-ferritin deficiency, dominant and recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the l-ferritin deficiency, dominant and recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

aromatase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aromatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?acat2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?acat2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia with isolated vitamin e deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, autosomal, due to deficiency of cyba Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset.

carnitine-acylcarnitine translocase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the carnitine-acylcarnitine translocase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

ulna and fibula, absence of, with severe limb deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ulna and fibula, absence of, with severe limb deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

glucocorticoid deficiency, due to acth unresponsiveness Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.

agammaglobulinemia and isolated hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the agammaglobulinemia and isolated hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.

17-alpha-hydroxylase/17,20-lyase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-2-macroglobulin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-2-macroglobulin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione peroxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

interleukin 1 receptor antagonist deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the interleukin 1 receptor antagonist deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

aromatic l-amino acid decarboxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aromatic l-amino acid decarboxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adenylosuccinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adenylosuccinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

acad9 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the acad9 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leukocyte adhesion deficiency, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukocyte adhesion deficiency, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 32b, monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 32b, monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

interleukin-2 receptor, alpha chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the interleukin-2 receptor, alpha chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, due to umph1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to ada deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

[aquaporin-1 deficiency] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [aquaporin-1 deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.

methionine adenosyltransferase deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

[alpha-actinin-3 deficiency] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [alpha-actinin-3 deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.

endplate acetylcholinesterase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the endplate acetylcholinesterase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenocorticotropic hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenocorticotropic hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?phosphoserine aminotransferase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?phosphoserine aminotransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

acyl-coa dehydrogenase, medium chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the acyl-coa dehydrogenase, medium chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

factor xi deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the factor xi deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

pyruvate dehydrogenase e1-alpha deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyruvate dehydrogenase e1-alpha deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

factor v and factor viii, combined deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the factor v and factor viii, combined deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperammonemia due to carbonic anhydrase va deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to g6pd deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-ketoglutarate dehydrogenase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-ketoglutarate dehydrogenase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase phenotype from the curated OMIM Gene-Disease Associations dataset.

interferon, alpha, deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the interferon, alpha, deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

platelet-activating factor acetylhydrolase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the platelet-activating factor acetylhydrolase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

acyl-coa dehydrogenase, short-chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the acyl-coa dehydrogenase, short-chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

autoinflammation, antibody deficiency, and immune dysregulation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoinflammation, antibody deficiency, and immune dysregulation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to adenylate kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?carnitine acetyltransferase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?carnitine acetyltransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to antithrombin iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

apoa-i and apoc-iii deficiency, combined Gene Set

From OMIM Gene-Disease Associations

genes associated with the apoa-i and apoc-iii deficiency, combined phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

acid-labile subunit, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the acid-labile subunit, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-2-plasmin inhibitor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-2-plasmin inhibitor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

aica-ribosiduria due to atic deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-methylacyl-coa racemase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-methylacyl-coa racemase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adenosine deaminase deficiency, partial Gene Set

From OMIM Gene-Disease Associations

genes associated with the adenosine deaminase deficiency, partial phenotype from the curated OMIM Gene-Disease Associations dataset.

apolipoprotein c-iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the apolipoprotein c-iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

n-terminal acetyltransferase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the n-terminal acetyltransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia due to adenosine kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

asparagine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the asparagine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

n-acetylglutamate synthase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the n-acetylglutamate synthase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?n-acetylaspartate deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?n-acetylaspartate deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

factor xi deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the factor xi deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

[amp deaminase deficiency, erythrocytic] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [amp deaminase deficiency, erythrocytic] phenotype from the curated OMIM Gene-Disease Associations dataset.

peroxisomal acyl-coa oxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the peroxisomal acyl-coa oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leukocyte adhesion deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukocyte adhesion deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

acetyl-coa carboxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the acetyl-coa carboxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

combined factor v and viii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined factor v and viii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

growth hormone deficiency with pituitary anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth hormone deficiency with pituitary anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-fetoprotein deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-fetoprotein deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adenine phosphoribosyltransferase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adenine phosphoribosyltransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adiponectin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adiponectin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?lysosomal acid phosphatase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?lysosomal acid phosphatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

plasminogen activator inhibitor-1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the plasminogen activator inhibitor-1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

phosphorylase kinase deficiency of liver and muscle, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the phosphorylase kinase deficiency of liver and muscle, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to triosephosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to hexokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

iron-refractory iron deficiency anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the iron-refractory iron deficiency anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema-cirrhosis, due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility due to acrosin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.

Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) Gene Set

From Reactome Pathways

proteins participating in the Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) pathway from the Reactome Pathways dataset.

Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) Gene Set

From Reactome Pathways

proteins participating in the Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) pathway from the Reactome Pathways dataset.

Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) Gene Set

From Reactome Pathways

proteins participating in the Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD) pathway from the Reactome Pathways dataset.

Bifunctional peroxisomal enzyme deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked ichthyosis with steryl-sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phosphoglycerate dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phosphoglycerate dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Galactosylceramide beta-galactosidase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Galactosylceramide beta-galactosidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Isolated 17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Isolated 17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sepiapterin reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyruvate dehydrogenase E2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase E2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coenzyme Q10 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of ribose-5-phosphate isomerase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of ribose-5-phosphate isomerase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kininogen deficiency, total Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kininogen deficiency, total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

6-pyruvoyl-tetrahydropterin synthase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 6-pyruvoyl-tetrahydropterin synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined oxidative phosphorylation deficiency 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined oxidative phosphorylation deficiency 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Creatine deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Creatine deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Birbeck granule deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Birbeck granule deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucocorticoid deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucocorticoid deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucocorticoid deficiency 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucocorticoid deficiency 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Properdin deficiency, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Properdin deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PROPERDIN DEFICIENCY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PROPERDIN DEFICIENCY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement factor d deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement factor d deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methylmalonyl-CoA epimerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methylmalonyl-CoA epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 8 deficiency type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 8 deficiency type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.