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GAD Gene-Disease Associations DatasetFrom Genetic Association Database Gene-disease associations curated from genetic association studies |
GAD High Level Gene-Disease Associations DatasetFrom Genetic Association Database Gene-disease associations curated from genetic association studies |
genetic anticipation with paternal anticipation bias Gene SetFrom HPO Gene-Disease Associations genes associated with the genetic anticipation with paternal anticipation bias phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Genetic Anticipation With Paternal Anticipation Bias Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genetic Anticipation With Paternal Anticipation Bias in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anticipation, genetic; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anticipation, genetic; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic anticipation Gene SetFrom HPO Gene-Disease Associations genes associated with the genetic anticipation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Anticipation, Genetic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Anticipation, Genetic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
serotonin transporter- pro-inflammatory bias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serotonin transporter- pro-inflammatory bias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bias Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term bias in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
antisense paternal transcript and loss of imprinting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antisense paternal transcript and loss of imprinting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
paternal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term paternal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Parent of origin effect on language impairment (paternal) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Parent of origin effect on language impairment (paternal) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
paternal imprinting Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the paternal imprinting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
paternal effect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the paternal effect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Uniparental Disomy, Paternal, Chromosome 14 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uniparental Disomy, Paternal, Chromosome 14 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paternal Uniparental Disomy Of Chromosome 6 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paternal Uniparental Disomy Of Chromosome 6 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paternal Uniparental Disomy Of Chromosome 20 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paternal Uniparental Disomy Of Chromosome 20 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paternal Alcoholism Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paternal Alcoholism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
paternal imprinting Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the paternal imprinting phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
paternal effect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the paternal effect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Parent of origin effect on receptive language ability (paternal) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parent of origin effect on receptive language ability (paternal) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parent of origin effect on language impairment (paternal) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parent of origin effect on language impairment (paternal) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
anticipation Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term anticipation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Anticipation, Psychological Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Anticipation, Psychological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Non-syndromic genetic deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Non-syndromic genetic deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Genetic Predisposition to Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Predisposition to Disease from the curated CTD Gene-Disease Associations dataset. |
Genetic Diseases, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Diseases, X-Linked 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. |
Translocation, Genetic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Translocation, Genetic from the curated CTD Gene-Disease Associations dataset. |
Recombination, Genetic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Recombination, Genetic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
autosomal genetic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autosomal genetic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
genetic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease genetic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
autosomal genetic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autosomal genetic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
genetic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease genetic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
autosomal genetic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autosomal genetic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
genetic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease genetic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
down syndrome; hirschsprung disease; nondisjunction, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease down syndrome; hirschsprung disease; nondisjunction, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
down syndrome; nondisjunction, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease down syndrome; nondisjunction, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
agammaglobulinemia; genetic diseases, x-linked Gene SetFrom GAD Gene-Disease Associations genes associated with the disease agammaglobulinemia; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, non-hodgkin; lymphoma, non-hodgkin's; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, non-hodgkin; lymphoma, non-hodgkin's; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recombination, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recombination, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic predisposition to disease; mouth neoplasms; neoplasms, squamous cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease; mouth neoplasms; neoplasms, squamous cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; diabetes mellitus; genetic predisposition to disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus; genetic predisposition to disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic predisposition to disease; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus 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. |
genetic markers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic markers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; leukemia, pre-b-cell; precursor b-cell lymphoblastic leukemia-lymphoma; precursor cell lymphoblastic leukemia-lymphoma; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; leukemia, pre-b-cell; precursor b-cell lymphoblastic leukemia-lymphoma; precursor cell lymphoblastic leukemia-lymphoma; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, x-linked; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, x-linked; lupus erythematosus, systemic; systemic lupus erythematosus 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. |
psoriasis; skin diseases, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease psoriasis; skin diseases, genetic 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. |
genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease 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. |
abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic 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, x-linked; rett syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, x-linked; rett syndrome 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. |
charcot-marie-tooth disease; genetic diseases, x-linked Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic polymorphisms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic polymorphisms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; genetic predisposition to disease 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. |
lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary restenosis; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary restenosis; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; skin diseases, genetic; vitiligo Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; skin diseases, genetic; vitiligo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic polymorphism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic polymorphism 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. |
fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes complications; diabetes mellitus, type 2; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes complications; diabetes mellitus, type 2; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cyp1a1 genetic polymorphisms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cyp1a1 genetic polymorphisms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic polymorphism of cytochrome p450 2a6 and the body status of iron stores Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic polymorphism of cytochrome p450 2a6 and the body status of iron stores in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; genetic predisposition to disease 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. |
chromosome breakage; cleft lip; cleft palate; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome breakage; cleft lip; cleft palate; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome inversion; leukemia, myeloid; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome inversion; leukemia, myeloid; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term genetic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of genetic imprinting Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of genetic imprinting biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of gene expression by genetic imprinting Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of gene expression by genetic imprinting biological process from the curated GO Biological Process Annotations 2015 dataset. |
genetic imprinting Gene SetFrom GO Biological Process Annotations 2015 genes participating in the genetic imprinting biological process from the curated GO Biological Process Annotations 2015 dataset. |
autosomal genetic disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease autosomal genetic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
genetic disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease genetic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Skin Diseases, Genetic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Genetic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genetic Predisposition to Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genetic Predisposition to Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genetic Determinism Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genetic Determinism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Nondisjunction, Genetic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Nondisjunction, Genetic 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. |
Genetic Diseases, Y-Linked Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genetic Diseases, Y-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Translocation, Genetic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Translocation, Genetic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genetic Diseases, X-Linked Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genetic Diseases, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genetic suppressor element-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Genetic suppressor element-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
genetic imprinting Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the genetic imprinting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
transcription-genetic Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term transcription-genetic in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Genetic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Recurrent Myoglobinuria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Recurrent Myoglobinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Amyloid Angiopathy, Genetic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Amyloid Angiopathy, Genetic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Transient Congenital Hypothyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Transient Congenital Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gene Genetic Abnormality Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gene Genetic Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Hyperferritinemia Without Iron Overload Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genetic Hyperferritinemia Without Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of genetic imprinting Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of genetic imprinting biological process from the curated GO Biological Process Annotations 2023 dataset. |
genetic imprinting Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the genetic imprinting phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Genetic causes of porto sinusoidal vascular disease Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Genetic causes of porto sinusoidal vascular disease pathway from the WikiPathways Pathways 2024 dataset. |
Autosomal genetic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal genetic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Genetic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Genetic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Genetic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Genetic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal genetic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autosomal genetic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Genetic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Genetic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal genetic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal genetic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sarcoma with BCOR genetic alterations Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sarcoma with BCOR genetic alterations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Rare genetic deafness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare genetic deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genetic transient congenital hypothyroidism Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic transient congenital hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nonsyndromic genetic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic genetic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Renal tubular dysgenesis of genetic origin Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal tubular dysgenesis of genetic origin phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genetic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genetic non-acquired premature ovarian failure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic non-acquired premature ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Rare genetic intellectual disability Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare genetic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genetic developmental and epileptic encephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic developmental and epileptic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Midgestational circulating levels of PCBs (fetal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational circulating levels of PCBs (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Midgestational circulating levels of PBDEs (fetal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational circulating levels of PBDEs (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to antiepileptic drugs in genetic generalized epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antiepileptic drugs in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to valproic acid in genetic generalized epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to lamotrigine in genetic generalized epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to levetiracetam in genetic generalized epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to levetiracetam in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to lamotrigine and valproic acid in genetic generalized epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine and valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Midgestational total 25-hydroxyvitamin D levels (maternal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational total 25-hydroxyvitamin D levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Midgestational total 25-hydroxyvitamin D levels (fetal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Midgestational cytokine/chemokine levels (maternal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational cytokine/chemokine levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neonatal cytokine/chemokine levels (maternal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Midgestational cytokine/chemokine levels (fetal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Midgestational cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neonatal cytokine/chemokine levels (fetal genetic effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist-to-hip ratio adjusted for BMI (recessive genetic model) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (recessive genetic model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist-to-hip ratio adjusted for BMI (additive genetic model) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (additive genetic model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Food allergy (maternal genetic effects) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Food allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Peanut allergy (maternal genetic effects) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peanut allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Milk allergy (maternal genetic effects) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Milk allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Egg allergy (maternal genetic effects) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Egg allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |