| Name |
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CTD Gene-Disease Associations DatasetFrom Comparative Toxicogenomics Database Disease-gene interactions from manually curated literature |
DISEASES Curated Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Disease gene evidence scores by manual literature curation |
DISEASES Experimental Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Disease gene evidence scores by integrating experimental data (GWAS) |
DISEASES Text-mining Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Gene-disease co-occurrence scores from text-mining biomedical abstracts |
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 |
GWASdb SNP-Disease Associations DatasetFrom GWASdb SNP-disease association p-values curated from published GWAS |
HPO Gene-Disease Associations DatasetPhenotype-causing gene mutations of human phenotypes from disease knowledgebases |
OMIM Gene-Disease Associations DatasetFrom Online Mendelian Inheritance in Man Disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications |
PhosphoSitePlus Phosphosite-Disease Associations DatasetFrom PhosphoSitePlus Disease-phosphosite associations curated from literature |
DisGeNET Gene-Disease Associations DatasetFrom DisGeNET Gene-disease associations sourced from curated repositories, GWAS catalogues, animal models and the scientific literature |
DISEASES Curated Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Disease gene evidence scores by manual literature curation |
DISEASES Experimental Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Disease gene evidence scores by integrating experimental data (GWAS) |
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Gene-disease co-occurrence scores from text-mining biomedical abstracts |
TFPT GeneTCF3 (E2A) fusion partner (in childhood Leukemia) Predicted to enable DNA binding activity. Involved in several processes, including apoptotic signaling pathway; chromatin remodeling; and regulation of nucleobase-containing compound metabolic process. Located in nucleoplasm. Part of Ino80 complex. [provided by Alliance of Genome Resources, Mar 2025] |
ECA1 Geneepilepsy, childhood absence 1 |
CELIAC8 GeneCeliac disease, susceptibility to, 8 |
CELIAC2 Geneceliac disease 2 |
CELIAC5 GeneCeliac disease, susceptibility to, 5 |
CELIAC6 GeneCeliac disease, susceptibility to, 6 |
CELIAC7 GeneCeliac disease, susceptibility to, 7 |
CELIAC9 GeneCeliac disease, susceptibility to, 9 |
CELIAC12 GeneCeliac disease, susceptibility to, 12 |
CELIAC13 GeneCeliac disease, susceptibility to, 13 |
CELIAC10 GeneCeliac disease, susceptibility to, 10 |
CELIAC11 GeneCeliac disease, susceptibility to, 11 |
Childhood Celiac Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, ulcerative; crohn disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft-versus-host disease; psoriasis; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Crohn's disease and celiac disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Crohn's disease and celiac disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Celiac Disease from the curated CTD Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Celiac Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
celiac disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease celiac disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
celiac disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease celiac disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
celiac disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease celiac disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
rheumatoid arthritis; preeclampsia; psoriasis; celiac disease; cervical cancer; psoriatic arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; preeclampsia; psoriasis; celiac disease; cervical cancer; psoriatic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; wegener's granulomatosis; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; wegener's granulomatosis; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; celiac disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; celiac disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, ulcerative; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; dermatitis herpetiformis; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; dermatitis herpetiformis; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; dermatitis, atopic; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; eczema allergic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; dermatitis, atopic; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; eczema allergic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; autoimmune diseases; celiac disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; autoimmune diseases; celiac disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; iga deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; diabetes mellitus, type 1; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; diabetes mellitus, type 1; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; celiac disease; diabetes mellitus, type 1; endocrine system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; celiac disease; diabetes mellitus, type 1; endocrine system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; celiac disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; celiac disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; celiac disease; liver failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; celiac disease; liver failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, ulcerative Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; celiac disease; myasthenia gravis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; celiac disease; myasthenia gravis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
psoriasis; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; common variable immunodeficiency; iga deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; common variable immunodeficiency; iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rheumatoid arthritis; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; down syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; down syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, microscopic; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, microscopic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Celiac disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Celiac disease and Rheumatoid arthritis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Celiac disease and Rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
celiac disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease celiac disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
celiac disease Gene SetFrom HPO Gene-Disease Associations genes associated with the celiac disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Celiac Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
{celiac disease, susceptibility to, 7} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 10} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 10} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 12} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 9} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 11} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 13} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{celiac disease, susceptibility to, 8} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {celiac disease, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Celiac Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Celiac Disease In Children Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Celiac Disease In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Form Of Celiac Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Form Of Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Celiac disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Celiac disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Celiac disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Celiac disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Celiac disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Celiac disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Celiac disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Celiac disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Celiac disease and Rheumatoid arthritis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Celiac disease and Rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Celiac disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Celiac disease or Rheumatoid arthritis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Celiac disease or Rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
celiac Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term celiac in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
celiac artery aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the celiac artery aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arteriovenous fistulas of celiac and mesenteric vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the arteriovenous fistulas of celiac and mesenteric vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
venous varicosities of celiac and mesenteric vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the venous varicosities of celiac and mesenteric vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Dilatation Of Celiac Artery Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilatation Of Celiac Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Venous Varicosities Of Celiac And Mesenteric Vessels Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Venous Varicosities Of Celiac And Mesenteric Vessels in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
absent celiac artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent celiac artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal celiac lymph node morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal celiac lymph node morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal celiac artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal celiac artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Celiac ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Celiac ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
childhood disintegrative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood disintegrative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infantile or childhood onset neurodegenerative disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
coronary artery disease; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; graves disease; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; disease susceptibility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease; hashimoto disease; hypothyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colitis; crohn disease; crohn's disease; disease models, animal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; graft vs host disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
North american indian childhood cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the North american indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epileptic encephalopathy, childhood-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alternating hemiplegia of childhood Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercalciuria, childhood, self-limiting Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercalciuria, childhood, self-limiting phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Childhood hypophosphatasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, childhood-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alternating hemiplegia of childhood 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset. |
North American Indian Childhood Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease North American Indian Childhood Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophies of Childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset. |
Mental Disorders Diagnosed in Childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset. |
Alternating hemiplegia of childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alternating hemiplegia of childhood from the curated CTD Gene-Disease Associations dataset. |
Arthropathy, progressive pseudorheumatoid, of childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset. |
Hypophosphatasia, Childhood Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Childhood from the curated CTD Gene-Disease Associations dataset. |
alternating hemiplegia of childhood Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
childhood medulloblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood oligodendroglioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood electroclinical syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood type dermatomyositis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood kidney neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood kidney cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood absence epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alternating hemiplegia of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood pilocytic astrocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
severe childhood thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe childhood thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood b-cell non-hodgkin's lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood b-cell non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute lymphoblastic leukemia (childhood) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute lymphoblastic leukemia (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood asthma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchial asthma (childhood only) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temperament in early childhood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease temperament in early childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood absence epilepsy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood b-cell precursor acute lymphoblastic leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood b-cell precursor acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophies of childhood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumors ; residential insecticide exposure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchial asthma (childhood & adult) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood atopic asthma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood atopic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, childhood acute lymphoblastic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute lymphoblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood acute lymphoblastic leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood-onset mood disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood-onset mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood maltreatment Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood maltreatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood asthma. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood asthma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma (childhood) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, childhood acute; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood idiopathic thrombocytopenic purpura. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma and ige in childhood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma and ige in childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma (childhood onset) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term childhood in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Fractional exhaled nitric oxide (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Asthma (childhood onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Acute lymphoblastic leukemia (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Intelligence (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Intelligence (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Asthma (childhood, severe) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
childhood-onset short-trunk short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections in infancy and early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
death in childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood-onset truncal obesity Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood-onset truncal obesity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset short-limb short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset sensorineural hearing impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of ability to walk in early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inability to walk by childhood/adolescence Gene SetFrom HPO Gene-Disease Associations genes associated with the inability to walk by childhood/adolescence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
platyspondyly (childhood) Gene SetFrom HPO Gene-Disease Associations genes associated with the platyspondyly (childhood) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Spinal Muscular Atrophies of Childhood Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lead Poisoning, Nervous System, Childhood Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lead Poisoning, Nervous System, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Schizophrenia, Childhood Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Schizophrenia, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
hypophosphatasia, childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypophosphatasia, childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
hepatocellular carcinoma, childhood type Gene SetFrom OMIM Gene-Disease Associations genes associated with the hepatocellular carcinoma, childhood type phenotype from the curated OMIM Gene-Disease Associations dataset. |
alternating hemiplegia of childhood 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, childhood absence, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
transient erythroblastopenia of childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the transient erythroblastopenia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, reducing body, x-linked, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
cirrhosis, north american indian childhood type Gene SetFrom OMIM Gene-Disease Associations genes associated with the cirrhosis, north american indian childhood type phenotype from the curated OMIM Gene-Disease Associations dataset. |
alternating hemiplegia of childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthropathy, progressive pseudorheumatoid, of childhood Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyarteritis nodosa, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyarteritis nodosa, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neurodegeneration with optic atrophy, childhood onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
{epilepsy, childhood absence, susceptibility to, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
epileptic encephalopathy, childhood-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
Childhood Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Liposarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Osteosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Neuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Kidney Wilms Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Myelodysplastic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Cytopenia Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Absence Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Megakaryoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Megakaryoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Alveolar Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Alveolar Soft Part Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Diffuse Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nephrotic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pilocytic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Soft Tissue Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Synovial Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Synovial Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood T Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Newly Diagnosed Childhood Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Newly Diagnosed Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Metastatic Childhood Soft Tissue Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Steroid Resistant Nephrotic Syndrome Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Steroid Resistant Nephrotic Syndrome Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Undifferentiated Pleomorphic Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Undifferentiated Pleomorphic Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Asthma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Supratentorial Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Monocytic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myelomonocytic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myelomonocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Burkitt Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hematopoietic Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hematopoietic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pre-B Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pre-B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Oligodendroglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ataxia With Central Nervous System Hypomyelinization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Craniopharyngioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Eosinophilic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Eosinophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Embryonal Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ganglioneuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioneuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Leiomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leiomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyarteritis Nodosa, Childhood-Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyarteritis Nodosa, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Stem Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Cerebral Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebral Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gliosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indian Childhood Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Angiosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alternating Hemiplegia Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Testicular Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ganglioglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Teratoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Childhood Caries Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Caries in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Promyelocytic Leukemia With Pml-Rara Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Promyelocytic Leukemia With Pml-Rara in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pleomorphic Xanthoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Xanthoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood T Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Epithelioid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Onset Dystonias Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Onset Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hypophosphatasia (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hypophosphatasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Subependymal Giant Cell Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Subependymal Giant Cell Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Oligoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Oligodendroglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Grade I Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade I Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Langerhans Cell Histiocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Langerhans Cell Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Atopic Dermatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Childhood Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pineoblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pineoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Monoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Clear Cell Sarcoma Of Soft Parts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Clear Cell Sarcoma Of Soft Parts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Immunoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Immunoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alternating Hemiplegia Of Childhood 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alternating Hemiplegia Of Childhood 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Diffuse Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Oligoastrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pilomyxoid Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilomyxoid Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Giant Cell Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Giant Cell Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Fibrillary Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Fibrillary Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Desmoplastic Small Round Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Kidney Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Atypical Teratoid/Rhabdoid Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Stem Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gliomatosis Cerebri Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliomatosis Cerebri in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Thyroid Gland Papillary Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Papillary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Ovarian Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ovarian Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Anaplastic Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Epithelioid Hemangioendothelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Hemangioendothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Brain Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Hemangiopericytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Hemangiopericytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Pleomorphic Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood L2 Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood L2 Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Solid Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Mesenchymal Chondrosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mesenchymal Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Erythroid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Erythroid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Liver Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontal Epilepsy, Benign, Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontal Epilepsy, Benign, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
North American Indian Childhood Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease North American Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercalciuria, Childhood, Self-Limiting Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercalciuria, Childhood, Self-Limiting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Transient Erythroblastopenia Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Transient Erythroblastopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Necrotizing Encephalopathy Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Basophilic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Basophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia In Remission Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nodular Sclerosis Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Sclerosis Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Botryoid-Type Embryonal Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Botryoid-Type Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Tic Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Psychosis, Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Psychosis, Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinal Muscular Atrophies Of Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophies Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Bronchiectasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Onset Of Psoriasis In Childhood (1-10 Years) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Onset Of Psoriasis In Childhood (1-10 Years) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Conduct Disorder, Childhood-Onset Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Conduct Disorder, Childhood-Onset Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gemistocytic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gemistocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood-Onset Spasticity With Hyperglycinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Spasticity With Hyperglycinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorea, Childhood-Onset, With Psychomotor Retardation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Childhood-Onset, With Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Diabetes Mellitus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Grade Ii Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Ii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Focal Epilepsy, Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Focal Epilepsy, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Benign Occipital Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Childhood Soft Tissue Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Gastrointestinal Stromal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progeria Syndrome, Childhood-Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progeria Syndrome, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Fibrous Histiocytoma Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Fibrous Histiocytoma Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Anaplastic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Small Intestinal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Small Intestinal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Colorectal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Colorectal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Thyroid Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Grade Iii Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Iii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Mixed Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mixed Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Childhood Epilepsy, Myoclonic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Epilepsy, Myoclonic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Supratentorial Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Early Childhood Onset Retinal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Unexplained Death In Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Leukemia In Remission Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Infratentorial Ependymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Infratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Disintegrative Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Disintegrative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Progressive Bulbar Palsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pneumonia Childhood Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pneumonia Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Choroid Plexus Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Choroid Plexus Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood-Onset Short-Trunk Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Cerebellar Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebellar Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Onset Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Death In Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Solid Neoplasm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood-Onset Truncal Obesity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood-Onset Truncal Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Overweight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Overweight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Aggression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Aggression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Selective Mutism Specific To Childhood And Adolescence Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Selective Mutism Specific To Childhood And Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infections In Infancy And Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk In Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Onset Short-Limb Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Convulsion In Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Convulsion In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Inability To Walk By Childhood/Adolescence Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inability To Walk By Childhood/Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Onset Sensorineural Hearing Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood electroclinical syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Childhood absence epilepsy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Alternating hemiplegia of childhood Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Progressive pseudorheumatoid arthropathy of childhood Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Childhood type dermatomyositis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Childhood type dermatomyositis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood acute lymphocytic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute lymphocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset asthma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood electroclinical syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood B-cell acute lymphoblastic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood B-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood fibrosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood low-grade glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood low-grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood kidney cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood absence epilepsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood medulloblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood acute myeloid leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood kidney cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood type dermatomyositis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Systemic Epstein-Barr virus positive T-cell lymphoma of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Systemic Epstein-Barr virus positive T-cell lymphoma of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood T-cell acute lymphoblastic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood T-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood brain stem neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood brain stem glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood osteosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood germ cell cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood astrocytic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood astrocytic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood infratentorial ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood leptomeningeal melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leptomeningeal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood angiosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood pilocytic astrocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alternating hemiplegia of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dystonia 28, childhood-onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 28, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood hypophosphatasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset neurodegeneration with brain atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood central nervous system embryonal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood hepatocellular carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hepatocellular carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood oligodendroglioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood acute megakaryoblastic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute megakaryoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dystonia 35, childhood-onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 35, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Progressive pseudorheumatoid arthropathy of childhood Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood liposarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood supratentorial ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood supratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood testicular germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant childhood germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant childhood germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood infratentorial neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood optic nerve glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood kidney angiomyolipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney angiomyolipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood ovarian dysgerminoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian dysgerminoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood ovarian germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood onset hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood apraxia of speech Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood apraxia of speech phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe early-childhood-onset retinal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glaucoma of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glaucoma of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alternating hemiplegia of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood hypophosphatasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood onset GLUT1 deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset GLUT1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood neoplasm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood neoplasm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe underweight in infancy childhood and adolescence Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe underweight in infancy childhood and adolescence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood ganglioglioma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood ganglioglioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood myocerebrohepatopathy spectrum Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood myocerebrohepatopathy spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive bulbar palsy of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood Onset Dystonias Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset Dystonias phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood kidney cell carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood kidney cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive childhood encephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood-onset motor and cognitive regression syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset motor and cognitive regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood absence epilepsy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary North American Indian childhood cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary North American Indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Death in childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sudden unexplained death in childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood-onset autosomal recessive myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
B-cell childhood acute lymphoblastic leukemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the B-cell childhood acute lymphoblastic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood onset sensorineural hearing impairment Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood Onset VCP-related Neurodevelopmental Disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset VCP-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Disabling pansclerotic morphea of childhood Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Disabling pansclerotic morphea of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Benign childhood epilepsy with centro-temporal spikes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cutaneous mastocytosis (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cutaneous mastocytosis (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
First fracture in long-term childhood cancer survivors (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the First fracture in long-term childhood cancer survivors (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood body mass index Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anthracycline-induced cardiotoxicity in childhood cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anthracycline-induced cardiotoxicity in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Obesity in adult survivors of childhood cancer exposed to cranial radiation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Obesity in adult survivors of childhood cancer not exposed to cranial radiation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer not exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Early childhood aggressive behavior Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early childhood aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Middle childhood and early adolescence aggressive behavior Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Middle childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood and early adolescence aggressive behavior Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood ear infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ear infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood maltreatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood maltreatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Meningococcal C functional antibody titers post childhood immunization Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meningococcal C functional antibody titers post childhood immunization phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood asthma exacerbations in long-acting beta2-agonist treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma exacerbations in long-acting beta2-agonist treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma (childhood onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma onset (childhood vs adult) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma onset (childhood vs adult) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood onset ulcerative colitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset ulcerative colitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute lymphoblastic leukemia (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fractional exhaled nitric oxide (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fasting plasma glucose (childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting plasma glucose (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma (time to childhood onset) in early life tobacco smoke exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) in early life tobacco smoke exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma (time to childhood onset) x early life tobacco smoke interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) x early life tobacco smoke interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood onset type 2 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood asthma with severe exacerbations Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute lymphoblastic leukemia in childhood (B cell precursor) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia in childhood (B cell precursor) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Premature menopause in childhood cancer survivors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Premature menopause in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood steroid-sensitive nephrotic syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood steroid-sensitive nephrotic syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to placebo treatment in childhood asthma (FVC change) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to placebo treatment in childhood asthma (FVC change) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Self-reported childhood asthma in adult smokers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Self-reported childhood asthma in adult smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Acute lymphoblastic leukemia (adult vs childhood) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (adult vs childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severe exacerbations in childhood asthma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe exacerbations in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood dental caries in primary teeth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in primary teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood dental caries in permanent teeth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in permanent teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Childhood absence epilepsy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cisplatin-induced hearing loss in childhood cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cisplatin-induced hearing loss in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
crohn disease; crohn's disease; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; melanoma; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; peripheral arterial disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; granuloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypercholesterolemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver disease; wilson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; dna damage; genomic instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hemochromatosis; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinson's disease ; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; cerebrovascular disease, ischemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; sarcoidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison's disease; graves' disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney disease; vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves ophthalmopathy; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; olfaction disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; autoimmune diseases; graves disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult-onset still disease; still's disease, adult-onset Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amnesia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; coronary disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; nervous system diseases; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; metabolic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; coronary restenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease parkinson's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cardiovascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; spondylitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; gastrointestinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; legg-perthes disease; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn's disease; ulcerative colitis; inflammatory bowel disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; postoperative complications; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; inflammation; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease; periodontal disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; heart failure; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; dyslipidemias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; disease susceptibility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; disease susceptibility; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertriglyceridemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; addison's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; ileal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinsons disease; alzheimers disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; coronary artery disease; hyperlipidemias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadaver; coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
common variable immunodeficiency; crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; intestinal obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic angiopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; dilatation, pathologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lewy body disease; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperlipidemias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sanhoff disease; tay-sachs disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; postoperative complications; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; delirium; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease/coronary artery disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; hallucinations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; growth disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; lewy body disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; lewy body disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; addison's disease; autoimmune diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroid disease; thyroid disease, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune 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. |
apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; neural tube defects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; spondylarthropathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylarthropathies 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. |
Cardiovascular Disease+Pulmonary Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiovascular Disease+Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parkinson's disease or first degree relation to individual with Parkinson's disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease or first degree relation to individual with Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alzheimer's disease or family history of Alzheimer's disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease or family history of Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors Gene SetFrom Biocarta Pathways proteins participating in the inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors pathway from the Biocarta Pathways dataset. |
deregulation of cdk5 in alzheimers disease Gene SetFrom Biocarta Pathways proteins participating in the deregulation of cdk5 in alzheimers disease pathway from the Biocarta Pathways dataset. |
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
Parkinson disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Premature coronary artery disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jakob-Creutzfeldt disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jakob-Creutzfeldt disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Maple syrup urine disease type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher's disease, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher's disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stargardt Disease 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stargardt Disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4H Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4J Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4G Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Norum disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Norum disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Salla disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Worth disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Worth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ménière's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ménière's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Maple syrup urine disease, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acute neuronopathic Gaucher's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IVF Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate E Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type IXa1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal recessive hypophosphatemic bone disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory bowel disease 25, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory bowel disease 25, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Moyamoya disease 6 with achalasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Moyamoya disease 6 with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IV, congenital neuromuscular Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4B3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4B1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brain small vessel disease with hemorrhage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
RRM2B-related mitochondrial disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phytanic acid storage disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 20, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasemia with bone disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chylomicron retention disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chylomicron retention disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Basal ganglia disease, biotin-responsive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Basal ganglia disease, biotin-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coronary artery disease, autosomal dominant 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 18 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Triglyceride storage disease with ichthyosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type II, infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2A1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IF Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type ID Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IC Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IB Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Schindler disease, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Schindler disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Schindler disease, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-pick disease, intermediate, protracted neurovisceral Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-pick disease, intermediate, protracted neurovisceral phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 6, autosomal recessive early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudo von Willebrand disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, juvenile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Darier disease, segmental Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Darier disease, segmental phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Naxos disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Naxos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, axonal, type 2s Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, axonal, type 2r Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, axonal, type 2q Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leiner disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leiner disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dowling-degos disease 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dowling-degos disease 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, atypical, due to saposin C deficiency Gene SetFrom 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. |
Hereditary factor II deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease 0, muscle Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease 0, muscle phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Subacute neuronopathic Gaucher's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Subacute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Testicular anomalies with or without congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lafora disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lafora disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease, type B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease, type A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease, type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type X Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tangier disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tangier disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cole disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cole disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 8, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 8, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXa2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXa2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Refsum disease, adult, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Refsum disease, adult, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital heart disease, multiple types, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Werdnig-Hoffmann disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Werdnig-Hoffmann disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 19, juvenile-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease type C2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease type C1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cholestanol storage disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-sachs disease, juvenile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-sachs disease, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IIIa Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stargardt disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stargardt disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor IX deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, adult type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, perinatal lethal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alexander's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alexander's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal arthrogryposis with anterior horn cell disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type 1A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dowling-Degos disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dowling-Degos disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-Sachs disease, B1 variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease, B1 variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mast cell disease, systemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mast cell disease, systemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease, adult type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease dominant intermediate 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neutral lipid storage disease with myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor XI deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Maple syrup urine disease type 1A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease XV Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease XV phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemoglobin H disease, nondeletional Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemoglobin H disease, nondeletional phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXb Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXc Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle eye brain disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Addison's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Addison's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital cystic disease of liver Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis and congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lhermitte-Duclos disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lhermitte-Duclos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kugelberg-Welander disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kugelberg-Welander disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Darier disease, acral hemorrhagic type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Wilson's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Wilson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate d Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate c Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IIIc Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IIIb Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease ganglioneuroblastoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease ganglioneuroblastoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oguchi's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oguchi's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kanzaki disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kanzaki disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic valve disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intermediate maple syrup urine disease type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intermediate maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fish-eye disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, chronic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease, infantile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Central core disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-Sachs disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2N Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2M Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-Sachs disease, variant AB Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease, variant AB phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sialic acid storage disease, severe infantile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2K Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
I cell disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the I cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoimmune disease, multisystem, infantile-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Medullary cystic kidney disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Danon disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Danon disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dent disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dent disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXd Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type V Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoimmune disease, syndromic multisystem Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, syndromic multisystem phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2J Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2P Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent Disease 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset. |
Pick Disease of the Brain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pick Disease of the Brain from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 10 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 12 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 13 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 14 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 15 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 18 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 18 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 19 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 19 from the curated CTD Gene-Disease Associations dataset. |
Huntington Disease-Like 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset. |
Parkinson disease 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson disease 9 from the curated CTD Gene-Disease Associations dataset. |
Oguchi disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease from the curated CTD Gene-Disease Associations dataset. |
Tay-Sachs Disease, AB Variant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset. |
Naxos disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Naxos disease from the curated CTD Gene-Disease Associations dataset. |
Huntington Disease-Like 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2K Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset. |
Carbamoyl-Phosphate Synthase I Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Chylomicron retention disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset. |
Cholesterol Ester Storage Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cholesterol Ester Storage Disease from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 6 from the curated CTD Gene-Disease Associations dataset. |
Addison Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Addison Disease from the curated CTD Gene-Disease Associations dataset. |
Alexander Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alexander Disease from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 16 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 16 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 17 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 17 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 7 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 4 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease 0, Liver Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Liver from the curated CTD Gene-Disease Associations dataset. |
Tangier Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tangier Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 1C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 26 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 26 from the curated CTD Gene-Disease Associations dataset. |
Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |