| Name |
|---|
inborn Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term inborn in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Megaloblastic anemia due to inborn errors of metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipid Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Pyruvate Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Purine-Pyrimidine Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Purine-Pyrimidine Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Amino Acid Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amino Acid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Genetic Diseases, Inborn Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Diseases, Inborn from the curated CTD Gene-Disease Associations dataset. |
Carbohydrate Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carbohydrate Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Brain Diseases, Metabolic, Inborn Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Diseases, Metabolic, Inborn from the curated CTD Gene-Disease Associations dataset. |
amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cockayne syndrome; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cockayne syndrome; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, aplastic; aplastic anemia; genetic diseases, inborn; graft vs host disease; hematologic neoplasms; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; aplastic anemia; genetic diseases, inborn; graft vs host disease; hematologic neoplasms; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amino acid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amino acid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; genetic diseases, inborn; lymphatic metastasis; mammary neoplasms; neoplasm invasiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; genetic diseases, inborn; lymphatic metastasis; mammary neoplasms; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypodontia; cleft lip; cleft palate; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypodontia; cleft lip; cleft palate; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, inborn; hearing impairment; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, dilated; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, inborn; syndrome; tetralogy of fallot Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; syndrome; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital megacolon; hirschsprung disease; urea cycle disorders, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital megacolon; hirschsprung disease; urea cycle disorders, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, inborn; polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism, inborn errors; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amino acid disorder, nos; amino acid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; metal metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; metal metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lipid Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lipid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Urea Cycle Disorders, Inborn Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Urea Cycle Disorders, Inborn phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Renal Tubular Transport, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Tubular Transport, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Purine-Pyrimidine Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Purine-Pyrimidine Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Steroid Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Steroid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Amino Acid Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Amino Acid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genetic Diseases, Inborn Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genetic Diseases, Inborn phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Metal Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Metal Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carbohydrate Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carbohydrate Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pyruvate Metabolism, Inborn Errors Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pyruvate Metabolism, Inborn Errors in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inborn Aminoaciduria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inborn Aminoaciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inborn error of immunity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inborn error of immunity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inborn mitochondrial myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inborn mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inborn glycerol kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inborn glycerol kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |