Aldehyde oxidase deficiency

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Results for "Aldehyde oxidase deficiency": 1001 gene sets

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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 Aldehyde Oxidase Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Deficiency Of Aldehyde Oxidase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
aldehyde oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the aldehyde oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Aldehyde oxidase/xanthine dehydrogenase, a/b hammerhead Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde oxidase/xanthine dehydrogenase, a/b hammerhead protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde oxidase/xanthine dehydrogenase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde oxidase/xanthine dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde oxidase/xanthine dehydrogenase, molybdopterin binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde oxidase/xanthine dehydrogenase, molybdopterin binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
aldehyde oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the aldehyde oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
aldehyde oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the aldehyde oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
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.
Glutaryl-CoA oxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutaryl-CoA oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sulfite oxidase deficiency, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sulfite oxidase deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Monoamine oxidase A deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Monoamine oxidase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cytochrome-c oxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cytochrome-c oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of xanthine oxidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of xanthine oxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency 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.
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Cytochrome-c Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cytochrome-c Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Sulfite oxidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sulfite oxidase deficiency from the curated CTD Gene-Disease Associations dataset.
cytochrome-c oxidase deficiency disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cytochrome-c oxidase deficiency disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cytochrome-c oxidase deficiency; leigh disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cytochrome-c oxidase deficiency; leigh disease 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.
sulfite oxidase deficiency Gene Set From HPO Gene-Disease Associations genes associated with the sulfite oxidase deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cytochrome-c Oxidase Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cytochrome-c Oxidase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
pyridoxamine 5'-phosphate oxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pyridoxamine 5'-phosphate oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
sulfite oxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the sulfite oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to cytochrome c oxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to cytochrome c oxidase deficiency 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.
[urate oxidase deficiency] Gene Set From OMIM Gene-Disease Associations genes associated with the [urate oxidase deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.
Peroxisomal Acyl-Coa Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Acyl-Coa Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Deficiency Of Oxidase Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Deficiency Of Oxidase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cytochrome-C Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cytochrome-C Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cytochrome C Oxidase I Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cytochrome C Oxidase I Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticosterone Methyl Oxidase Type I Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticosterone Methyl Oxidase Type I Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticosterone Methyl Oxidase Type Ii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticosterone Methyl Oxidase Type Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sulfite Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sulfite Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extraoral Halitosis Due To Methanethiol Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extraoral Halitosis Due To Methanethiol Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
cytochrome-c oxidase deficiency disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease cytochrome-c oxidase deficiency disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Isolated sulfite oxidase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Isolated sulfite oxidase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Pyridoxamine 5'-phosphate oxidase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pyridoxamine 5'-phosphate oxidase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Peroxisomal acyl-CoA oxidase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peroxisomal acyl-CoA oxidase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cytochrome-c oxidase deficiency disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cytochrome-c oxidase deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated sulfite oxidase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated sulfite oxidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peroxisomal acyl-CoA oxidase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peroxisomal acyl-CoA oxidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pyridoxamine 5'-phosphate oxidase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pyridoxamine 5'-phosphate oxidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acyl-CoA oxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acyl-CoA oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sulfite oxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Corticosterone methyl oxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Corticosterone methyl oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glutaryl-CoA oxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glutaryl-CoA oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
hexyl cinnamic aldehyde Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical hexyl cinnamic aldehyde from the curated CTD Gene-Chemical Interactions dataset.
caprylic aldehyde Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical caprylic aldehyde from the curated CTD Gene-Chemical Interactions dataset.
cinnamic aldehyde Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical cinnamic aldehyde from the curated CTD Gene-Chemical Interactions dataset.
hydratropic aldehyde Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical hydratropic aldehyde from the curated CTD Gene-Chemical Interactions dataset.
acetyl-valyl-isoleucyl-aspartyl-aldehyde Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical acetyl-valyl-isoleucyl-aspartyl-aldehyde from the curated CTD Gene-Chemical Interactions dataset.
benzyloxycarbonylleucyl-leucyl-leucine aldehyde Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical benzyloxycarbonylleucyl-leucyl-leucine aldehyde from the curated CTD Gene-Chemical Interactions dataset.
aldehyde Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term aldehyde in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
aldehyde catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the aldehyde catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular aldehyde metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular aldehyde metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
aldehyde biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the aldehyde biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
aldehyde dehydrogenase (nad) activity Gene Set From GO Molecular Function Annotations 2015 genes performing the aldehyde dehydrogenase (nad) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors Gene Set From GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set From GO Molecular Function Annotations 2015 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 2015 dataset.
betaine-aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the betaine-aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
transferase activity, transferring aldehyde or ketonic groups Gene Set From GO Molecular Function Annotations 2015 genes performing the transferase activity, transferring aldehyde or ketonic groups molecular function from the curated GO Molecular Function Annotations 2015 dataset.
aldehyde dehydrogenase [nad(p)+] activity Gene Set From GO Molecular Function Annotations 2015 genes performing the aldehyde dehydrogenase [nad(p)+] activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor Gene Set From GO Molecular Function Annotations 2015 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 2015 dataset.
3-chloroallyl aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the 3-chloroallyl aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set From GO Molecular Function Annotations 2015 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 2015 dataset.
aldehyde-lyase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the aldehyde-lyase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Gentisate aldehyde Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Gentisate aldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.
Citalopram aldehyde Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Citalopram aldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.
Betaine aldehyde Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Betaine aldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.
trans-3-Chloroallyl aldehyde Gene Set From HMDB Metabolites of Enzymes interacting proteins for the trans-3-Chloroallyl aldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.
cis-3-Chloroallyl aldehyde Gene Set From HMDB Metabolites of Enzymes interacting proteins for the cis-3-Chloroallyl aldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.
Perillyl aldehyde Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Perillyl aldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.
Aldehyde dehydrogenase, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde dehydrogenase domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde dehydrogenase, glutamic acid active site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase, glutamic acid active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde dehydrogenase N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde dehydrogenase NAD(P)-dependent Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase NAD(P)-dependent protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde dehydrogenase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde dehydrogenase, cysteine active site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde dehydrogenase, cysteine active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Aldehyde/histidinol dehydrogenase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Aldehyde/histidinol dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
aldehyde catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the aldehyde catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
aldehyde biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the aldehyde biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to aldehyde Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to aldehyde biological process from the curated GO Biological Process Annotations 2023 dataset.
3-chloroallyl aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the 3-chloroallyl aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2023 genes performing the aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
aldehyde dehydrogenase [NAD(P)+] activity Gene Set From GO Molecular Function Annotations 2023 genes performing the aldehyde dehydrogenase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor Gene Set From GO Molecular Function Annotations 2023 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 2023 dataset.
betaine-aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the betaine-aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
long-chain-aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the long-chain-aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
medium-chain-aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the medium-chain-aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
20-aldehyde-leukotriene B4 20-monooxygenase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the 20-aldehyde-leukotriene B4 20-monooxygenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
aldehyde-lyase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the aldehyde-lyase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set From GO Molecular Function Annotations 2023 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 2023 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set From GO Molecular Function Annotations 2023 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 2023 dataset.
decreased aldehyde dehydrogenase activity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased aldehyde dehydrogenase activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Gentisate aldehyde Gene Set From MW Enzyme Metabolite Associations interacting proteins for Gentisate aldehyde metabolite from the MW Gene Metabolite Associations dataset.
Betaine aldehyde Gene Set From MW Enzyme Metabolite Associations interacting proteins for Betaine aldehyde metabolite from the MW Gene Metabolite Associations dataset.
aldehyde catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the aldehyde catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
aldehyde biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the aldehyde biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to aldehyde Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to aldehyde biological process from the curated GO Biological Process Annotations 2025 dataset.
3-chloroallyl aldehyde dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the 3-chloroallyl aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
aldehyde dehydrogenase [NAD(P)+] activity Gene Set From GO Molecular Function Annotations 2025 genes performing the aldehyde dehydrogenase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
aldehyde-lyase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the aldehyde-lyase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
betaine-aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the betaine-aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
medium-chain fatty aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the medium-chain fatty aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
20-aldehyde-leukotriene B4 20-monooxygenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the 20-aldehyde-leukotriene B4 20-monooxygenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor Gene Set From GO Molecular Function Annotations 2025 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 2025 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set From GO Molecular Function Annotations 2025 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 2025 dataset.
oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set From GO Molecular Function Annotations 2025 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 2025 dataset.
fatty aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the fatty aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
BETAINE ALDEHYDE CHLORIDE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the BETAINE ALDEHYDE CHLORIDE drug from theDGIdb Drug Targets 2026 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.
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.
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.
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.
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.
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.
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.
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.
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set From Reactome Pathways 2014 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 2014 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 2014 proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Set From Reactome Pathways 2024 proteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset.
nadph oxidase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nadph oxidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
nadph oxidase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nadph oxidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Cytochrome c oxidase (EC 1.9.3.1), mitochondrial Gene Set From CORUM Protein Complexes proteins in the Cytochrome c oxidase (EC 1.9.3.1), mitochondrial protein complex from the CORUM Protein Complexes dataset.
platelet monoamine oxidase b activity Gene Set From GAD Gene-Disease Associations genes associated with the disease platelet monoamine oxidase b activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deficient cytochrome c oxidase assembly Gene Set From GAD Gene-Disease Associations genes associated with the disease deficient cytochrome c oxidase assembly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vascular nad(p)h oxidase activity Gene Set From GAD Gene-Disease Associations genes associated with the disease vascular nad(p)h oxidase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nadph oxidase Gene Set From GAD Gene-Disease Associations genes associated with the disease nadph oxidase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
oxidase Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term oxidase in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of nad(p)h oxidase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of nad(p)h oxidase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
fatty acid beta-oxidation using acyl-coa oxidase Gene Set From GO Biological Process Annotations 2015 genes participating in the fatty acid beta-oxidation using acyl-coa oxidase biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of d-amino-acid oxidase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of d-amino-acid oxidase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of nad(p)h oxidase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of nad(p)h oxidase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of d-amino-acid oxidase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of d-amino-acid oxidase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of nad(p)h oxidase activity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of nad(p)h oxidase activity biological process from the curated GO Biological Process Annotations 2015 dataset.
nadph oxidase complex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the nadph oxidase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
15-oxoprostaglandin 13-oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the 15-oxoprostaglandin 13-oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
pyridoxamine-phosphate oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the pyridoxamine-phosphate oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
lathosterol oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the lathosterol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
sarcosine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the sarcosine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
aliphatic-amine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the aliphatic-amine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
xanthine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the xanthine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
l-pipecolate oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the l-pipecolate oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
nad(p)h oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the nad(p)h oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
glyoxylate oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the glyoxylate oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
c-4 methylsterol oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the c-4 methylsterol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
very-long-chain-(s)-2-hydroxy-acid oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the very-long-chain-(s)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
superoxide-generating nadph oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the superoxide-generating nadph oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
glycolate oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the glycolate oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
(s)-2-hydroxy-acid oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the (s)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
l-amino-acid oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the l-amino-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
aspartate oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the aspartate oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
long-chain-alcohol oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
prenylcysteine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the prenylcysteine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
primary amine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the primary amine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
caffeine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the caffeine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
coproporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the coproporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
cytochrome-c oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the cytochrome-c oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
d-aspartate oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the d-aspartate oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
heme-copper terminal oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the heme-copper terminal oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
oxygen-dependent protoporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the oxygen-dependent protoporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
d-amino-acid oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the d-amino-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
palmitoyl-coa oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the palmitoyl-coa oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
protoporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the protoporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
sulfite oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the sulfite oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
electron transporter, transferring electrons from coqh2-cytochrome c reductase complex and cytochrome c oxidase complex activity Gene Set From GO Molecular Function Annotations 2015 genes performing the electron transporter, transferring electrons from coqh2-cytochrome c reductase complex and cytochrome c oxidase complex activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
protein-lysine 6-oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the protein-lysine 6-oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
acyl-coa oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the acyl-coa oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
superoxide-generating nadph oxidase activator activity Gene Set From GO Molecular Function Annotations 2015 genes performing the superoxide-generating nadph oxidase activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
histamine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the histamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
methylputrescine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the methylputrescine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
medium-chain-(s)-2-hydroxy-acid oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the medium-chain-(s)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
pristanoyl-coa oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the pristanoyl-coa oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
diamine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the diamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
flavin-linked sulfhydryl oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the flavin-linked sulfhydryl oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
polyamine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the polyamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
propane-1,3-diamine oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the propane-1,3-diamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
thiol oxidase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the thiol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
decreased activity of nadph oxidase Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of nadph oxidase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of cytochrome c oxidase in muscle tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of cytochrome c oxidase in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Pyridoxine 5'-phosphate oxidase, dimerisation, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxine 5'-phosphate oxidase, dimerisation, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N2/N3-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2/N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome C oxidase subunit II, transmembrane domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome C oxidase subunit II, transmembrane domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase copper chaperone Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase copper chaperone protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protoporphyrinogen oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protoporphyrinogen oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit 6C Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit 6C protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
FAD linked oxidase, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FAD linked oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
NADPH oxidase subunit p47Phox, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the NADPH oxidase subunit p47Phox, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pyridoxamine 5'-phosphate oxidase, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxamine 5'-phosphate oxidase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase assembly protein CtaG/Cox11, domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase assembly protein CtaG/Cox11, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit III domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit III domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA dehydrogenase/oxidase, N-terminal and middle domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA dehydrogenase/oxidase, N-terminal and middle domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dual oxidase maturation factor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dual oxidase maturation factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome C oxidase, subunit VIIB, domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome C oxidase, subunit VIIB, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
ERV/ALR sulfhydryl oxidase domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the ERV/ALR sulfhydryl oxidase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit IV Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit IV protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coproporphyrinogen III oxidase, oxygen-independent related Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coproporphyrinogen III oxidase, oxygen-independent related protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit I Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit I protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit I domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit I domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Flavin amine oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Flavin amine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lysyl oxidase, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysyl oxidase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA oxidase/dehydrogenase, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA oxidase/dehydrogenase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit VIIc Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit VIIc protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit VIa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit VIa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Pyridoxamine 5'-phosphate oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Pyridoxamine 5'-phosphate oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit III, 4-helical bundle Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit III, 4-helical bundle protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit Va/VI Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit Va/VI protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coproporphyrinogen III oxidase, aerobic Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coproporphyrinogen III oxidase, aerobic protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Galactose oxidase, beta-propeller Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Galactose oxidase, beta-propeller protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit III Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit III protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit VIa, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit VIa, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit II C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit II C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit VIIa Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit VIIa protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Vanillyl-alcohol oxidase, C-terminal subdomain 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Vanillyl-alcohol oxidase, C-terminal subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit VIII/photosystem I reaction centre subunit IX Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit VIII/photosystem I reaction centre subunit IX protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Amine oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Amine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase assembly protein PET191 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase assembly protein PET191 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
FAD-linked oxidase-like, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FAD-linked oxidase-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit II Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit II protein domain from the InterPro Predicted Protein Domain Annotations dataset.
D-amino-acid oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the D-amino-acid oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Proline oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase assembly protein CtaG/Cox11 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase assembly protein CtaG/Cox11 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dual oxidase 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dual oxidase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA dehydrogenase/oxidase, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA dehydrogenase/oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-coenzyme A oxidase, N-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-coenzyme A oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome C oxidase, subunit VIIB Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome C oxidase, subunit VIIB protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase biogenesis protein Cmc1-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase biogenesis protein Cmc1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA dehydrogenase/oxidase C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA dehydrogenase/oxidase C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit 8 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N2-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA oxidase, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit Vb, zinc binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit Vb, zinc binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit Vb Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit Vb protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synthesis of cytochrome c oxidase, Sco1/Sco2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synthesis of cytochrome c oxidase, Sco1/Sco2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Prenyltransferase/squalene oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Prenyltransferase/squalene oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Protoporphyrinogen oxidase, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Protoporphyrinogen oxidase, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
D-amino acid oxidase, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the D-amino acid oxidase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Coproporphyrinogen III oxidase, conserved site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Coproporphyrinogen III oxidase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Lysyl oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysyl oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase assembly protein COX14 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase assembly protein COX14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase assembly protein COX16 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase assembly protein COX16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Copper amine oxidase, N3-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multicopper oxidase, copper-binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dihydroxyindole-2-carboxylic acid oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dihydroxyindole-2-carboxylic acid oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
FAD-linked oxidase, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the FAD-linked oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Galactose oxidase/kelch, beta-propeller Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Galactose oxidase/kelch, beta-propeller protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Prenylcysteine oxidase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Prenylcysteine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Zinc-finger domain of monoamine-oxidase A repressor R1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc-finger domain of monoamine-oxidase A repressor R1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
NADPH oxidase 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the NADPH oxidase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
NADPH oxidase 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the NADPH oxidase 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
NADPH oxidase 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the NADPH oxidase 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multicopper oxidase, type 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multicopper oxidase, type 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multicopper oxidase, type 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, type 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit VIIa-related, mitochondrial Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit VIIa-related, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit VIb Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit VIb protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Sarcosine oxidase, monomeric Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Sarcosine oxidase, monomeric protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase, subunit I, copper-binding site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit I, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome c oxidase subunit IV family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase subunit IV family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cytochrome oxidase assembly protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome oxidase assembly protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
D-amino acid oxidase activator Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the D-amino acid oxidase activator protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Dual oxidase 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dual oxidase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
oxidase Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term oxidase in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Amine Oxidase reactions Gene Set From Reactome Pathways 2014 proteins participating in the Amine Oxidase reactions pathway from the Reactome Pathways dataset.
Enzymatic degradation of Dopamine by monoamine oxidase Gene Set From Reactome Pathways 2014 proteins participating in the Enzymatic degradation of Dopamine by monoamine oxidase pathway from the Reactome Pathways dataset.
Cytochrome C Oxidase-Negative Muscle Fibers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cytochrome C Oxidase-Negative Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Activity Of Nadph Oxidase Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Activity Of Nadph Oxidase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
mitochondrial cytochrome c oxidase assembly Gene Set From GO Biological Process Annotations 2023 genes participating in the mitochondrial cytochrome c oxidase assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of cytochrome-c oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of cytochrome-c oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
fatty acid beta-oxidation using acyl-CoA oxidase Gene Set From GO Biological Process Annotations 2023 genes participating in the fatty acid beta-oxidation using acyl-CoA oxidase biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of primary amine oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of primary amine oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of NAD(P)H oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of NAD(P)H oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of NAD(P)H oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of NAD(P)H oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of D-amino-acid oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of D-amino-acid oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of cytochrome-c oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of cytochrome-c oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of NAD(P)H oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of NAD(P)H oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of D-amino-acid oxidase activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of D-amino-acid oxidase activity biological process from the curated GO Biological Process Annotations 2023 dataset.
NADPH oxidase complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the NADPH oxidase complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
flavin-linked sulfhydryl oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the flavin-linked sulfhydryl oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
cytochrome-c oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the cytochrome-c oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
NAD(P)H oxidase H2O2-forming activity Gene Set From GO Molecular Function Annotations 2023 genes performing the NAD(P)H oxidase H2O2-forming activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
primary amine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the primary amine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
superoxide-generating NADPH oxidase activator activity Gene Set From GO Molecular Function Annotations 2023 genes performing the superoxide-generating NADPH oxidase activator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
superoxide-generating NAD(P)H oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the superoxide-generating NAD(P)H oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
caffeine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the caffeine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
thiol oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the thiol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
palmitoyl-CoA oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the palmitoyl-CoA oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
D-amino-acid oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the D-amino-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
diamine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the diamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
monoamine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the monoamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
coproporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the coproporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
acyl-CoA oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the acyl-CoA oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
xanthine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the xanthine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
oxygen-dependent protoporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the oxygen-dependent protoporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
long-chain-alcohol oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
20-hydroxy-leukotriene B4 omega oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the 20-hydroxy-leukotriene B4 omega oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
methanethiol oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the methanethiol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
C-4 methylsterol oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the C-4 methylsterol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
polyamine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the polyamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
15-oxoprostaglandin 13-oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the 15-oxoprostaglandin 13-oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
formylglycine-generating oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the formylglycine-generating oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
L-amino-acid oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the L-amino-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
D-aspartate oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the D-aspartate oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
pyridoxamine-phosphate oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the pyridoxamine-phosphate oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
(S)-2-hydroxy-acid oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the (S)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
sarcosine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the sarcosine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
L-pipecolate oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the L-pipecolate oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
prenylcysteine oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the prenylcysteine oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
glyoxylate oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the glyoxylate oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
pristanoyl-CoA oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the pristanoyl-CoA oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
sulfite oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the sulfite oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
protoporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the protoporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
increased NAD(P)H oxidase activity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased NAD(P)H oxidase activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased monoamine oxidase activity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased monoamine oxidase activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Amine Oxidase reactions Gene Set From Reactome Pathways 2024 proteins participating in the Amine Oxidase reactions pathway from the Reactome Pathways 2024 dataset.
Enzymatic degradation of Dopamine by monoamine oxidase Gene Set From Reactome Pathways 2024 proteins participating in the Enzymatic degradation of Dopamine by monoamine oxidase pathway from the Reactome Pathways 2024 dataset.
mitochondrial cytochrome c oxidase assembly Gene Set From GO Biological Process Annotations 2025 genes participating in the mitochondrial cytochrome c oxidase assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
fatty acid beta-oxidation using acyl-CoA oxidase Gene Set From GO Biological Process Annotations 2025 genes participating in the fatty acid beta-oxidation using acyl-CoA oxidase biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of primary amine oxidase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of primary amine oxidase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of NAD(P)H oxidase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of NAD(P)H oxidase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of cytochrome-c oxidase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of cytochrome-c oxidase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of NAD(P)H oxidase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of NAD(P)H oxidase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of cytochrome-c oxidase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of cytochrome-c oxidase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of NAD(P)H oxidase activity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of NAD(P)H oxidase activity biological process from the curated GO Biological Process Annotations 2025 dataset.
NADPH oxidase complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the NADPH oxidase complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
flavin-dependent sulfhydryl oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the flavin-dependent sulfhydryl oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
NAD(P)H oxidase H2O2-forming activity Gene Set From GO Molecular Function Annotations 2025 genes performing the NAD(P)H oxidase H2O2-forming activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
primary methylamine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the primary methylamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
superoxide-generating NADPH oxidase activator activity Gene Set From GO Molecular Function Annotations 2025 genes performing the superoxide-generating NADPH oxidase activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
superoxide-generating NAD(P)H oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the superoxide-generating NAD(P)H oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
superoxide-generating NADPH oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the superoxide-generating NADPH oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
caffeine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the caffeine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
thiol oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the thiol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
palmitoyl-CoA oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the palmitoyl-CoA oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
D-amino-acid oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the D-amino-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
putrescine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the putrescine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
diamine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the diamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
histamine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the histamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
monoamine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the monoamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
coproporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the coproporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
acyl-CoA oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the acyl-CoA oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
xanthine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the xanthine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
oxygen-dependent protoporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the oxygen-dependent protoporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain-alcohol oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
20-hydroxy-leukotriene B4 omega oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the 20-hydroxy-leukotriene B4 omega oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
methanethiol oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the methanethiol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
15-oxoprostaglandin 13-oxidase [NAD(P)+] activity Gene Set From GO Molecular Function Annotations 2025 genes performing the 15-oxoprostaglandin 13-oxidase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
C-4 methylsterol oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the C-4 methylsterol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
polyamine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the polyamine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
formylglycine-generating oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the formylglycine-generating oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
L-amino-acid oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the L-amino-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
D-aspartate oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the D-aspartate oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
pyridoxamine phosphate oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the pyridoxamine phosphate oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
spermine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the spermine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
(S)-2-hydroxy-acid oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the (S)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
sarcosine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the sarcosine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
L-pipecolate oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the L-pipecolate oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
prenylcysteine oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the prenylcysteine oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
glyoxylate oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the glyoxylate oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
pristanoyl-CoA oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the pristanoyl-CoA oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
sulfite oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the sulfite oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
protoporphyrinogen oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the protoporphyrinogen oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
NADPH oxidase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the NADPH oxidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
NADPH oxidase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the NADPH oxidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Glycolate oxidase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Glycolate oxidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cytochrome o ubiquinol oxidase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytochrome o ubiquinol oxidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Sarcosine oxidase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Sarcosine oxidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
MONOAMINE OXIDASE INHIBITOR Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOAMINE OXIDASE INHIBITOR drug from theDGIdb Drug Targets 2026 dataset.
XANTHINE OXIDASE INHIBITOR Gene Set From DGIdb Drug Targets 2026 interacting proteins for the XANTHINE OXIDASE INHIBITOR drug from theDGIdb Drug Targets 2026 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Testosterone 17-beta-dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testosterone 17-beta-dehydrogenase 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.
Deficiency of 2-methylbutyryl-CoA dehydrogenase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of 2-methylbutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of isobutyryl-CoA dehydrogenase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of isobutyryl-CoA dehydrogenase 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.
Cerebral folate deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral folate deficiency 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.
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Partial hypoxanthine-guanine phosphoribosyltransferase 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.
Carnitine palmitoyltransferase I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex I 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.
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary C1 esterase inhibitor deficiency - dysfunctional factor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipase deficiency combined Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipase deficiency combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
5-Oxoprolinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 5-Oxoprolinase 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.
Proopiomelanocortin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proopiomelanocortin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrinsic factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrinsic factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
21-hydroxylase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 21-hydroxylase deficiency 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.
Corticosterone methyloxidase type 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corticosterone methyloxidase type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thiopurine methyltransferase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thiopurine methyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
METHYLCOBALAMIN DEFICIENCY, cblG TYPE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the METHYLCOBALAMIN DEFICIENCY, cblG TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine palmitoyltransferase II deficiency, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lactate dehydrogenase b deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lactate dehydrogenase b deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of 3-hydroxyacyl-CoA dehydrogenase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of 3-hydroxyacyl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Plasminogen deficiency, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Plasminogen deficiency, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase 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, 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.
Biotinidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Biotinidase deficiency 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.
Hypohidrotic ectodermal dysplasia with immune deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypohidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of phosphoserine phosphatase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of phosphoserine phosphatase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Isolated growth hormone deficiency type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of butyryl-CoA dehydrogenase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of butyryl-CoA dehydrogenase 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.
3 Methylcrotonyl-CoA carboxylase 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3 Methylcrotonyl-CoA carboxylase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of hyaluronoglucosaminidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of hyaluronoglucosaminidase 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.
Pyruvate dehydrogenase phosphatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase phosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 22 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor V deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor V 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.
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamate formiminotransferase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutamate formiminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoglycemia with deficiency of glycogen synthetase in the liver Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoglycemia with deficiency of glycogen synthetase in the liver 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.
Follicle-stimulating hormone deficiency, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Follicle-stimulating hormone deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ganglioside sialidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ganglioside sialidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C1q deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C1q deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interferon gamma receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interferon gamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet glycoprotein IV deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet glycoprotein IV deficiency 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.
Triosephosphate isomerase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Triosephosphate isomerase 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.
Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase 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.
Hereditary factor II deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial complex III deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor xiii, a subunit, deficiency of Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor xiii, a subunit, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial complex III deficiency, nuclear type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial complex III deficiency, nuclear type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylcrotonyl CoA carboxylase 2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylcrotonyl CoA carboxylase 2 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.
Leigh syndrome due to mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple sulfatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corticosteroid-binding globulin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corticosteroid-binding globulin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corticosterone methyloxidase type 2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corticosterone methyloxidase type 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 9 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holocarboxylase synthetase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holocarboxylase synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
2,4-Dienoyl-CoA reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 2,4-Dienoyl-CoA reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of glycerate kinase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of glycerate kinase 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.
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of galactokinase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of galactokinase 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.
PROPERDIN DEFICIENCY, TYPE III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PROPERDIN DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carboxylesterase 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carboxylesterase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Purine-nucleoside phosphorylase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Purine-nucleoside phosphorylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 6 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 6 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.
Inosine triphosphatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inosine triphosphatase 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.
Homocysteinemia due to MTHFR deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of pyrroline-5-carboxylate reductase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of pyrroline-5-carboxylate reductase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency due to ficolin 3 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sarcosine dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sarcosine dehydrogenase 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.
Branched-chain ketoacid dehydrogenase kinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branched-chain ketoacid dehydrogenase kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
L-ferritin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the L-ferritin deficiency 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.
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor 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.
Hepatic lipase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hepatic lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor X deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase 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.
Pyruvate dehydrogenase E3-binding protein deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E3-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor IX deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease 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.
Vitamin k-dependent clotting factors, combined deficiency of, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of iodide peroxidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of iodide peroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycosylphosphatidylinositol deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycosylphosphatidylinositol deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitamin k-dependent clotting factors, combined deficiency of, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 2 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.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Caspase-8 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Caspase-8 deficiency 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.
Phosphoglycerate kinase 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Phosphoglycerate kinase 1 deficiency 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.
Enterokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enterokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coenzyme Q10 deficiency, primary, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coenzyme Q10 deficiency, primary, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coenzyme Q10 deficiency, primary, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coenzyme Q10 deficiency, primary, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 3 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.
Factor VII deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor VII 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.
Myeloperoxidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myeloperoxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial phosphate carrier deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial phosphate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor XI deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Porphobilinogen synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Porphobilinogen synthase 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.
IRAK4 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the IRAK4 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.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 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.
Cortisone reductase deficiency 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortisone reductase deficiency 2 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.
Pyruvate kinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyruvate kinase 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.
Dihydropyrimidinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dihydropyrimidinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dimethylglycine dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dimethylglycine dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of hydroxymethylglutaryl-CoA lyase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of hydroxymethylglutaryl-CoA lyase 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.
Isovaleryl-CoA dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Isovaleryl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd59 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd59 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.
Deficiency of ferroxidase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of ferroxidase 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.
Deficiency of steroid 11-beta-monooxygenase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of steroid 11-beta-monooxygenase 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.
Dopamine beta hydroxylase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dopamine beta hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Butyrylcholinesterase deficiency, fluoride-resistant, japanese type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Butyrylcholinesterase deficiency, fluoride-resistant, japanese type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
UDPglucose-4-epimerase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the UDPglucose-4-epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Homocystinuria due to MTHFR deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria due to MTHFR 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.
Insulin-like growth factor I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-like growth factor I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex II deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyruvate carboxylase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyruvate carboxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gluthathione synthetase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gluthathione synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fumarase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fumarase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of transaldolase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of transaldolase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial pyruvate carrier deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial pyruvate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyruvate dehydrogenase E1-beta deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E1-beta deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MASP2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MASP2 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.
Prekallikrein deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prekallikrein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chitotriosidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chitotriosidase 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.
Prothrombin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial trifunctional protein deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial trifunctional protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
GTP cyclohydrolase I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the GTP cyclohydrolase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of malonyl-CoA decarboxylase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of malonyl-CoA decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3 beta-Hydroxysteroid dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3 beta-Hydroxysteroid dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Succinate-semialdehyde dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Succinate-semialdehyde dehydrogenase deficiency 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.
Okt4 epitope deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Okt4 epitope 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.
Mitochondrial complex II deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mineralocorticoid deficiency, isolated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement 1s deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement 1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dihydropteridine reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dihydropteridine reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mannose-binding protein deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mannose-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucose transporter type 1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucose transporter type 1 deficiency syndrome 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.
Myd88 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myd88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd8 deficiency, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 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.
Fructose-biphosphatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fructose-biphosphatase 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.
Complement factor B deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement factor B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Obesity, severe, due to leptin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Beta-hydroxyisobutyryl-CoA deacylase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Beta-hydroxyisobutyryl-CoA deacylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor VIII deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proline dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proline dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor H deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor H deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamine deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital 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.
Glycine N-methyltransferase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycine N-methyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ornithine carbamoyltransferase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ornithine carbamoyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sucrase-isomaltase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sucrase-isomaltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cholesterol monooxygenase (side-chain cleaving) deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cholesterol monooxygenase (side-chain cleaving) deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fucosyltransferase 6 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fucosyltransferase 6 deficiency 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.
Pituitary hormone deficiency, combined, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of butyrylcholine esterase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of butyrylcholine esterase 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.
Protein S deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Protein S deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of glycerol kinase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of glycerol kinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Urocanate hydratase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Urocanate hydratase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
4-Hydroxyphenylpyruvate dioxygenase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 4-Hydroxyphenylpyruvate dioxygenase deficiency 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.
Factor xiii, b subunit, deficiency of Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor xiii, b subunit, deficiency of 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.
Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency 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.
Deficiency of (R)-20-hydroxysteroid dehydrogenase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of (R)-20-hydroxysteroid dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prolidase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prolidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of beta-ureidopropionase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of beta-ureidopropionase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of guanidinoacetate methyltransferase Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of guanidinoacetate methyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYD88 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYD88 Deficiency from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease 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.
Platelet Glycoprotein IV Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Glycoprotein IV Deficiency from the curated CTD Gene-Disease Associations dataset.
Mitochondrial Phosphate Carrier Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Phosphate Carrier 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.
Prekallikrein Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prekallikrein Deficiency from the curated CTD Gene-Disease Associations dataset.
Methylenetetrahydrofolate reductase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylenetetrahydrofolate reductase deficiency from the curated CTD Gene-Disease Associations dataset.
6-pyruvoyl-tetrahydropterin synthase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 6-pyruvoyl-tetrahydropterin synthase deficiency from the curated CTD Gene-Disease Associations dataset.
Factor XI Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XI Deficiency from the curated CTD Gene-Disease Associations dataset.
Carnitine palmitoyl transferase 1A deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine palmitoyl transferase 1A deficiency 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.
THYROTROPIN-RELEASING HORMONE DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THYROTROPIN-RELEASING HORMONE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Carbamoyl-Phosphate Synthase I Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Tyrosine Kinase 2 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tyrosine Kinase 2 Deficiency from the curated CTD Gene-Disease Associations dataset.
Properdin deficiency, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Properdin deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.
COENZYME Q10 DEFICIENCY, PRIMARY, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COENZYME Q10 DEFICIENCY, PRIMARY, 1 from the curated CTD Gene-Disease Associations dataset.
Glutathione synthetase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutathione synthetase deficiency from the curated CTD Gene-Disease Associations dataset.
Glucocorticoid Deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid Deficiency 2 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.
Combined Oxidative Phosphorylation Deficiency 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 3 from the curated CTD Gene-Disease Associations dataset.
Proopiomelanocortin Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Proopiomelanocortin 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.
Glucocorticoid Deficiency 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid Deficiency 3 from the curated CTD Gene-Disease Associations dataset.
Intrinsic Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intrinsic Factor 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.
Combined Oxidative Phosphorylation Deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 2 from the curated CTD Gene-Disease Associations dataset.
Plasminogen Deficiency, Type I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Plasminogen Deficiency, Type I from the curated CTD Gene-Disease Associations dataset.
IgA Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease IgA Deficiency from the curated CTD Gene-Disease Associations dataset.
Lipase deficiency combined Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipase deficiency combined 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.
DNA Repair-Deficiency Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DNA Repair-Deficiency Disorders from the curated CTD Gene-Disease Associations dataset.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Enterokinase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Enterokinase Deficiency from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Late-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Late-Onset from the curated CTD Gene-Disease Associations dataset.
Lactase Deficiency, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactase Deficiency, Congenital 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.
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.
Beta ketothiolase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta ketothiolase deficiency from the curated CTD Gene-Disease Associations dataset.
Transaldolase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Transaldolase Deficiency 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.
Succinyl-CoA:3-oxoacid CoA transferase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Succinyl-CoA:3-oxoacid CoA transferase deficiency from the curated CTD Gene-Disease Associations dataset.
CD8 Deficiency, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.
Neuraminidase 1 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase 1 deficiency 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.
Vitamin B 12 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin B 12 Deficiency from the curated CTD Gene-Disease Associations dataset.
Isolated Growth Hormone Deficiency, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type II from the curated CTD Gene-Disease Associations dataset.
Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.
Familial HDL deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency 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.
Methylcobalamin Deficiency, CblG Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylcobalamin Deficiency, CblG Type from the curated CTD Gene-Disease Associations dataset.
Flaujeac factor deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Flaujeac factor deficiency from the curated CTD Gene-Disease Associations dataset.
Ribose 5-Phosphate Isomerase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ribose 5-Phosphate Isomerase Deficiency from the curated CTD Gene-Disease Associations dataset.
Pyruvate dehydrogenase phosphatase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate dehydrogenase phosphatase deficiency from the curated CTD Gene-Disease Associations dataset.
VLCAD deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VLCAD deficiency from the curated CTD Gene-Disease Associations dataset.
18-Hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 18-Hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Creatine deficiency, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Creatine deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.
Mitochondrial Complex III Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Complex III Deficiency from the curated CTD Gene-Disease Associations dataset.
PROPROTEIN CONVERTASE 1/3 DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROPROTEIN CONVERTASE 1/3 DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
dopamine beta hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease dopamine beta hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Ehlers-Danlos syndrome caused by tenascin-X deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos syndrome caused by tenascin-X deficiency from the curated CTD Gene-Disease Associations dataset.
Growth mental deficiency syndrome of Myhre Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth mental deficiency syndrome of Myhre from the curated CTD Gene-Disease Associations dataset.
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset.
Ornithine Carbamoyltransferase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ornithine Carbamoyltransferase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Protein Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Protein Deficiency 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.
3-methylcrotonyl CoA carboxylase 2 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-methylcrotonyl CoA carboxylase 2 deficiency from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I 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.
Thiopurine S methyltranferase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thiopurine S methyltranferase deficiency 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.
3-Hydroxyacyl-CoA Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-Hydroxyacyl-CoA Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency from the curated CTD Gene-Disease Associations dataset.
Isolated Growth Hormone Deficiency, Type IB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type IB from the curated CTD Gene-Disease Associations dataset.
Vitamin A Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin A Deficiency from the curated CTD Gene-Disease 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.
Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset.
Phosphoglycerate Kinase 1 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoglycerate Kinase 1 Deficiency from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II 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.
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 from the curated CTD Gene-Disease Associations dataset.
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 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.
Pyruvate Dehydrogenase E2 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase E2 Deficiency from the curated CTD Gene-Disease Associations dataset.
Phosphoglycerate Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoglycerate Dehydrogenase 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.
Vitamin D Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin D Deficiency from the curated CTD Gene-Disease Associations dataset.
Factor V Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor V 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.
Pyruvate Dehydrogenase Complex Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase Complex Deficiency Disease 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 X Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor X 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.
Holocarboxylase Synthetase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Holocarboxylase Synthetase Deficiency 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.
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 from the curated CTD Gene-Disease Associations dataset.
Dimethylglycine Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dimethylglycine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Pituitary Hormone Deficiency, Combined, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Hormone Deficiency, Combined, 1 from the curated CTD Gene-Disease Associations dataset.
Pituitary Hormone Deficiency, Combined, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Hormone Deficiency, Combined, 2 from the curated CTD Gene-Disease Associations dataset.
Trehalase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trehalase Deficiency from the curated CTD Gene-Disease Associations dataset.
Guanidinoacetate methyltransferase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Guanidinoacetate methyltransferase 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.
Phosphoenolpyruvate carboxykinase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoenolpyruvate carboxykinase deficiency from the curated CTD Gene-Disease Associations dataset.
17-Hydroxysteroid Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 17-Hydroxysteroid Dehydrogenase Deficiency from the curated CTD 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.
Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency from the curated CTD Gene-Disease Associations dataset.
D-BIFUNCTIONAL PROTEIN DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease D-BIFUNCTIONAL PROTEIN 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.
Biotinidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Biotinidase Deficiency from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT C1r/C1s 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.
Phosphoenolpyruvate carboxykinase 2 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoenolpyruvate carboxykinase 2 deficiency from the curated CTD Gene-Disease Associations dataset.
Glycine N-Methyltransferase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycine N-Methyltransferase 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.
Magnesium Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Magnesium Deficiency from the curated CTD Gene-Disease Associations dataset.
2-Methylbutyryl-CoA Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 2-Methylbutyryl-CoA Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Glycosylphosphatidylinositol deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycosylphosphatidylinositol deficiency from the curated CTD Gene-Disease Associations dataset.
Factor Xiii, A Subunit, Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor Xiii, A Subunit, Deficiency Of from the curated CTD Gene-Disease Associations dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor 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.
Isobutyryl-CoA dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Isobutyryl-CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Dihydropyrimidine Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dihydropyrimidine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Corticosteroid-Binding Globulin Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corticosteroid-Binding Globulin Deficiency from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency 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.
Factor XIII, B Subunit, Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XIII, B Subunit, Deficiency Of 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.
GLUT1 DEFICIENCY SYNDROME 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLUT1 DEFICIENCY SYNDROME 2 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.
Specific Granule Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Specific Granule Deficiency from the curated CTD Gene-Disease Associations dataset.
Insulin-Like Growth Factor I Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insulin-Like Growth Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement component 5 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement component 5 deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Lactate dehydrogenase deficiency type A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactate dehydrogenase deficiency type A from the curated CTD Gene-Disease Associations dataset.
Pyruvate Dehydrogenase E3-Binding Protein Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase E3-Binding Protein Deficiency 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.
Cortisone reductase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cortisone reductase deficiency from the curated CTD Gene-Disease Associations dataset.
NADH cytochrome B5 reductase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NADH cytochrome B5 reductase deficiency from the curated CTD Gene-Disease Associations dataset.
3b-Hydroxysteroid Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3b-Hydroxysteroid Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Thiamine Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thiamine Deficiency from the curated CTD Gene-Disease Associations dataset.
Mitochondrial Complex II Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Complex II Deficiency from the curated CTD Gene-Disease Associations dataset.
Sucrase-isomaltase deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sucrase-isomaltase deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Systemic carnitine deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Systemic carnitine deficiency from the curated CTD Gene-Disease Associations dataset.
Gamma-cystathionase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gamma-cystathionase deficiency from the curated CTD Gene-Disease Associations dataset.
Pituitary Hormone Deficiency, Combined, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Hormone Deficiency, Combined, 4 from the curated CTD Gene-Disease Associations dataset.
Combined Saposin Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Saposin Deficiency from the curated CTD Gene-Disease Associations dataset.
Radial Ray Deficiency, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Radial Ray Deficiency, X-Linked from the curated CTD Gene-Disease Associations dataset.
Beta-Ureidopropionase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta-Ureidopropionase Deficiency from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 5 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 4 from the curated CTD Gene-Disease Associations dataset.
Protein C Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Protein C Deficiency from the curated CTD Gene-Disease Associations dataset.
succinic semialdehyde dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease succinic semialdehyde dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Carboxypeptidase N Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carboxypeptidase N Deficiency from the curated CTD Gene-Disease Associations dataset.
Purine Nucleoside Phosphorylase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purine Nucleoside Phosphorylase Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 4, Partial Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 4, Partial Deficiency Of from the curated CTD Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 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.
Factor XIII Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XIII 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.
Fructose-1,6-Diphosphatase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fructose-1,6-Diphosphatase Deficiency from the curated CTD Gene-Disease Associations dataset.
MASP2 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MASP2 Deficiency from the curated CTD Gene-Disease Associations dataset.
2,4-Dienoyl-CoA Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 2,4-Dienoyl-CoA Reductase Deficiency 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.
Complement Factor H Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Factor H Deficiency from the curated CTD Gene-Disease Associations dataset.
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT 2 DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 2 DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
TRANSCOBALAMIN II DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRANSCOBALAMIN II DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Prolidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prolidase 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.
Dihydropyrimidinase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dihydropyrimidinase Deficiency from the curated CTD Gene-Disease Associations dataset.
Deficiency Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deficiency Diseases from the curated CTD Gene-Disease Associations dataset.
BISPHOSPHOGLYCERATE MUTASE DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BISPHOSPHOGLYCERATE MUTASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Vitamin E Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin E Deficiency from the curated CTD Gene-Disease Associations dataset.
PROTHROMBIN DEFICIENCY, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROTHROMBIN DEFICIENCY, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Infantile from the curated CTD Gene-Disease Associations dataset.
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency from the curated CTD Gene-Disease Associations dataset.
CD59 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD59 Deficiency from the curated CTD Gene-Disease Associations dataset.
Myeloperoxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myeloperoxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Methylmalonyl-CoA Epimerase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonyl-CoA Epimerase Deficiency from the curated CTD Gene-Disease Associations dataset.
Mevalonate Kinase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mevalonate Kinase Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Factor I Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.
Beta-Hydroxyisobutyryl CoA Deacylase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta-Hydroxyisobutyryl CoA Deacylase Deficiency from the curated CTD Gene-Disease Associations dataset.
Hyaluronidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyaluronidase Deficiency 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.
3-methylcrotonyl CoA carboxylase 1 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-methylcrotonyl CoA carboxylase 1 deficiency from the curated CTD Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Lysosomal beta-mannosidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lysosomal beta-mannosidase deficiency 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.
Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.
Glutamine deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutamine deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Pyruvate Kinase Deficiency of Red Cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Kinase Deficiency of Red Cells from the curated CTD Gene-Disease Associations dataset.
Factor VII Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor VII 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.
IRAK4 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease IRAK4 Deficiency from the curated CTD Gene-Disease Associations dataset.
Butyrylcholinesterase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Butyrylcholinesterase 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.
Pyruvate Carboxylase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Carboxylase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Complement Component 6 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 6 Deficiency from the curated CTD Gene-Disease Associations dataset.
Glutamate formiminotransferase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutamate formiminotransferase deficiency from the curated CTD Gene-Disease Associations dataset.
Factor XII Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XII 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.
Urocanase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Urocanase 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.
Ectodermal dysplasia, hypohidrotic, with immune deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, hypohidrotic, with immune deficiency from the curated CTD Gene-Disease Associations dataset.
Immunoglobulin a deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunoglobulin a deficiency 2 from the curated CTD Gene-Disease Associations dataset.
Immunoglobulin a deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunoglobulin a deficiency 1 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.
Glucosephosphate Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucosephosphate Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Mitochondrial complex I deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial complex I deficiency from the curated CTD Gene-Disease Associations dataset.
Follicle-stimulating hormone deficiency, isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Follicle-stimulating hormone deficiency, isolated from the curated CTD Gene-Disease Associations dataset.
Split-hand/foot malformation with long bone deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset.
Immunologic Deficiency Syndromes Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunologic Deficiency Syndromes from the curated CTD Gene-Disease Associations dataset.
protein s deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease protein s deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
systemic primary carnitine deficiency disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease systemic primary carnitine deficiency disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
purine nucleoside phosphorylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease purine nucleoside phosphorylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
alpha 1-antitrypsin deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease alpha 1-antitrypsin deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
holocarboxylase synthetase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease holocarboxylase synthetase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
gamma chain deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease gamma chain deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
pyruvate decarboxylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pyruvate decarboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
serine deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease serine deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebral creatine deficiency syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
complement deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease complement deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
agat deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease agat deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
prothrombin deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease prothrombin deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
complement factor i deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease complement factor i deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glucosephosphate dehydrogenase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glucosephosphate dehydrogenase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
protein c deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease protein c deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dihydropyrimidine dehydrogenase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dihydropyrimidine dehydrogenase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
biotinidase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease biotinidase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
beta-ketothiolase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease beta-ketothiolase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ornithine carbamoyltransferase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ornithine carbamoyltransferase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
factor v deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease factor v deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ornithine translocase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ornithine translocase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cd40 ligand deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cd40 ligand deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
b cell deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease b cell deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
3-methylcrotonyl-coa carboxylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease 3-methylcrotonyl-coa carboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
phgdh deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease phgdh deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
succinic semialdehyde dehydrogenase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease succinic semialdehyde dehydrogenase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
adenosine deaminase deficiency Gene Set From DISEASES Curated Gene-Disease Association 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 Association Evidence Scores genes involed in the disease antithrombin iii deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple carboxylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
iron deficiency anemia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease iron deficiency anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
nutritional deficiency disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease nutritional deficiency disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
choline deficiency disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease choline deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mhc class ii deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mhc class ii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
t lymphocyte deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease t lymphocyte deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leukocyte-adhesion deficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association 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.
familial lipoprotein lipase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
complement deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease complement deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urethral intrinsic sphincter deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urethral intrinsic sphincter deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital intrinsic factor deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital intrinsic factor deficiency 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 Association 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.
fructose-1,6-bisphosphatase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fructose-1,6-bisphosphatase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
coenzyme q10 deficiency disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease coenzyme q10 deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pyruvate decarboxylase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pyruvate decarboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
psat deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease psat deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carbamoyl phosphate synthetase i deficiency disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carbamoyl phosphate synthetase i deficiency disease 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 Association 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 Association 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 Association 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.
factor xiii deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factor xiii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
b cell linker protein deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease b cell linker protein 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 Association 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.
cd3delta deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cd3delta deficiency 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 Association 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.
protein s deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease protein s deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gamma chain deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gamma chain deficiency 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 Association 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.
intestinal disaccharidase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal disaccharidase 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 Association 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.
cd40 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cd40 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 Association 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.
dna ligase iv deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dna ligase iv deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cd45 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cd45 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
factor viii deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factor viii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cd3zeta deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cd3zeta deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
factor vii deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factor vii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
selective igg deficiency disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease selective igg deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
factor xii deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factor xii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cd40 ligand deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cd40 ligand deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
serine deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease serine 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 Association 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.

Harmonizome 3.0

aldehyde oxidase deficiency Gene Set

Deficiency Of Aldehyde Oxidase Gene Set

aldehyde oxidase activity Gene Set

Aldehyde oxidase/xanthine dehydrogenase, a/b hammerhead Gene Set

Aldehyde oxidase/xanthine dehydrogenase Gene Set

Aldehyde oxidase Gene Set

Aldehyde oxidase/xanthine dehydrogenase, molybdopterin binding Gene Set

aldehyde oxidase activity Gene Set

aldehyde oxidase activity Gene Set

Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene Set

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

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

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

Glutaryl-CoA oxidase deficiency Gene Set

Sulfite oxidase deficiency, isolated Gene Set

Monoamine oxidase A deficiency Gene Set

Cytochrome-c oxidase deficiency Gene Set

Deficiency of xanthine oxidase Gene Set

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set

Peroxisomal ACYL-COA oxidase deficiency Gene Set

Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Gene Set

Cytochrome-c Oxidase Deficiency Gene Set

Sulfite oxidase deficiency Gene Set

cytochrome-c oxidase deficiency disease Gene Set

cytochrome-c oxidase deficiency; leigh disease Gene Set

hypertrophic cardiomyopathy and cytochrome c oxidase deficiency Gene Set

leigh syndrome and cytochrome c oxidase deficiency Gene Set

sulfite oxidase deficiency Gene Set

Cytochrome-c Oxidase Deficiency Gene Set

pyridoxamine 5'-phosphate oxidase deficiency Gene Set

sulfite oxidase deficiency Gene Set

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set

leigh syndrome due to cytochrome c oxidase deficiency Gene Set

peroxisomal acyl-coa oxidase deficiency Gene Set

[urate oxidase deficiency] Gene Set

Peroxisomal Acyl-Coa Oxidase Deficiency Gene Set

Deficiency Of Oxidase Gene Set

Cytochrome-C Oxidase Deficiency Gene Set

Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene Set

Cytochrome C Oxidase I Deficiency Gene Set

Corticosterone Methyl Oxidase Type I Deficiency Gene Set

Corticosterone Methyl Oxidase Type Ii Deficiency Gene Set

Sulfite Oxidase Deficiency Gene Set

Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Gene Set

Extraoral Halitosis Due To Methanethiol Oxidase Deficiency Gene Set

cytochrome-c oxidase deficiency disease Gene Set

Isolated sulfite oxidase deficiency Gene Set

Pyridoxamine 5'-phosphate oxidase deficiency Gene Set

Peroxisomal acyl-CoA oxidase deficiency Gene Set

cytochrome-c oxidase deficiency disease Gene Set

Isolated sulfite oxidase deficiency Gene Set

Peroxisomal acyl-CoA oxidase deficiency Gene Set

Pyridoxamine 5'-phosphate oxidase deficiency Gene Set

Acyl-CoA oxidase deficiency Gene Set

Sulfite oxidase deficiency Gene Set

Corticosterone methyl oxidase deficiency Gene Set

Glutaryl-CoA oxidase deficiency Gene Set

hexyl cinnamic aldehyde Gene Set

caprylic aldehyde Gene Set

cinnamic aldehyde Gene Set

hydratropic aldehyde Gene Set

acetyl-valyl-isoleucyl-aspartyl-aldehyde Gene Set

benzyloxycarbonylleucyl-leucyl-leucine aldehyde Gene Set

aldehyde Gene Set

aldehyde catabolic process Gene Set

cellular aldehyde metabolic process Gene Set

aldehyde biosynthetic process Gene Set

aldehyde dehydrogenase (nad) activity Gene Set

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

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

betaine-aldehyde dehydrogenase activity Gene Set

transferase activity, transferring aldehyde or ketonic groups Gene Set

aldehyde dehydrogenase [nad(p)+] activity Gene Set

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

3-chloroallyl aldehyde dehydrogenase activity Gene Set

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

aldehyde-lyase activity Gene Set

Gentisate aldehyde Gene Set