Name

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with Woolly hair and keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset.

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, with woolly hair and keratoderma Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, with woolly hair and keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; dcm - dilated cardiomyopathy; heart failure; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; dcm - dilated cardiomyopathy; heart failure; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; cardiomyopathy, dilated; dcm - dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; cardiomyopathy, dilated; dcm - dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia; postoperative complications; rheumatic heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia; postoperative complications; rheumatic heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; chagas cardiomyopathy; chagas disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; chagas cardiomyopathy; chagas disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin fragility woolly hair syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

WOOLLY HAIR, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease WOOLLY HAIR, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Skin Fragility-Woolly Hair Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skin Fragility-Woolly Hair Syndrome from the curated CTD Gene-Disease Associations dataset.

Woolly hair, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Woolly hair, congenital from the curated CTD Gene-Disease Associations dataset.

woolly hair Gene Set

From HPO Gene-Disease Associations

genes associated with the woolly hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

woolly hair, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

skin fragility-woolly hair syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the skin fragility-woolly hair syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

Dilated cardiomyopathy 1LL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1LL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary dilated cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, 1nn Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, 1nn phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, 1u Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1EE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1EE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 3B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1DD Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1DD phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1S Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1W Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1W phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1X Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1Y Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1Y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1Z Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1Z phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1CC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1CC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1FF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1FF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1HH Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1HH phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy with left ventricular noncompaction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy with left ventricular noncompaction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy 1JJ Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy 1JJ phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CARDIOMYOPATHY, DILATED, 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, DILATED, 3B from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1FF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1FF from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1DD Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1DD from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 2a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 2a from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1K from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1AA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1AA from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1C from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1D from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1E from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1J from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1N Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1N from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1M Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1M from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1V Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1V from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1g Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1g from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1i Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1i from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1o Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1o from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1s Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1s from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1p Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1p from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1q Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1q from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1w Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1w from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1u Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1u from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1z Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1z from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1x Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1x from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1y Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1y from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1CC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1CC from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1l Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1l from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1BB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1BB from the curated CTD Gene-Disease Associations dataset.

Familial dilated cardiomyopathy Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Dilated, 1t Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1t from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated, 1EE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Dilated, 1EE from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Dilated Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Cardiomyopathy, Dilated in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

dilated cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

dilated cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

nonfamilial idiopathic dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonfamilial idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; coxsackievirus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; coxsackievirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, idiopathic dilated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, idiopathic dilated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomegaly; cardiomyopathy, dilated; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomegaly; cardiomyopathy, dilated; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

idiopathic dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; genetic diseases, inborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; cardiomyopathy, dilated; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; cardiomyopathy, dilated; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked dilated cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Dilated cardiomyopathy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

dilated cardiomyopathy Gene Set

From GWASdb SNP-Disease Associations

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

dilated cardiomyopathy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the dilated cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

dilated cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the dilated cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cardiomyopathy, Dilated Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

dilated cardiomyopathy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cardiomyopathy, dilated 1c Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated 1c phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1cc Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1cc phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1ee Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1ee phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

?cardiomyopathy, dilated, 1aa Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiomyopathy, dilated, 1aa phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1hh Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1hh phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1jj Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1jj phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1ll Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1ll phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1nn Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1nn phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1bb Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1bb phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1dd Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1dd phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

?cardiomyopathy, dilated, 1t Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiomyopathy, dilated, 1t phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1ff Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1ff phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1k Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1k phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1i Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1i phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1n Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1n phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1o Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1o phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1l Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1l phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1m Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1m phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1r Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1r phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1s Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1s phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1p Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1p phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1q Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1q phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1v Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1v phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1w Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1w phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1u Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1u phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1z Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1z phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1x Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1x phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1y Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1y phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1kk Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1kk phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1j Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1j phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1ii phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1gg Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1gg phenotype from the curated OMIM Gene-Disease Associations dataset.

?cardiac conduction disease with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1mm Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1mm phenotype from the curated OMIM Gene-Disease Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

keratosis linearis with ichthyosis congenita and sclerosing keratoderma Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratosis linearis with ichthyosis congenita and sclerosing keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.

erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper ige Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper ige phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

dilated hair follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated hair follicle infundibulum Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated hair follicle infundibulum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Cardiomyopathy:Cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy:Cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

cardiomyopathy, hypertrophic; cardiomyopathy, restrictive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; cardiomyopathy, restrictive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

woolly Gene Set

From GeneRIF Biological Term Annotations

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

[skin/hair/eye pigmentation 6, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 6, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 9, dark/light hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 10, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 10, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[hair morphology 1, hair thickness] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hair morphology 1, hair thickness] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, black/nonblack hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, black/nonblack hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 2, red hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 7, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 7, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 1, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 1, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Palmoplantar keratoderma, nonepidermolytic, focal or diffuse Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Palmoplantar keratoderma, nonepidermolytic, focal or diffuse phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Palmoplantar keratoderma, nonepidermolytic, focal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Palmoplantar keratoderma, nonepidermolytic, focal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mutilating keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mutilating keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Keratoderma palmoplantar deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Keratoderma palmoplantar deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Palmoplantar keratoderma, nagashima type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Palmoplantar keratoderma, nagashima type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Keratoderma, Palmoplantar Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratoderma, Palmoplantar from the curated CTD Gene-Disease Associations dataset.

Keratoderma palmoplantar deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratoderma palmoplantar deafness from the curated CTD Gene-Disease Associations dataset.

Keratoderma, Palmoplantar, Epidermolytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratoderma, Palmoplantar, Epidermolytic from the curated CTD Gene-Disease Associations dataset.

PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL from the curated CTD Gene-Disease Associations dataset.

Palmoplantar Keratoderma, Nonepidermolytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Palmoplantar Keratoderma, Nonepidermolytic from the curated CTD Gene-Disease Associations dataset.

nonepidermolytic palmoplantar keratoderma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

keratoderma Gene Set

From GeneRIF Biological Term Annotations

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

diffuse palmoplantar keratoderma Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse palmoplantar keratoderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

honeycomb palmoplantar keratoderma Gene Set

From HPO Gene-Disease Associations

genes associated with the honeycomb palmoplantar keratoderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy palmoplantar keratoderma Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy palmoplantar keratoderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

palmoplantar keratoderma Gene Set

From HPO Gene-Disease Associations

genes associated with the palmoplantar keratoderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nonepidermolytic palmoplantar keratoderma Gene Set

From HPO Gene-Disease Associations

genes associated with the nonepidermolytic palmoplantar keratoderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Keratoderma, Palmoplantar Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

palmoplantar keratoderma, bothnian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma, bothnian type phenotype from the curated OMIM Gene-Disease Associations dataset.

palmoplantar keratoderma, nonepidermolytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma, nonepidermolytic phenotype from the curated OMIM Gene-Disease Associations dataset.

palmoplantar keratoderma, nonepidermolytic, focal or diffuse Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma, nonepidermolytic, focal or diffuse phenotype from the curated OMIM Gene-Disease Associations dataset.

palmoplantar keratoderma, nonepidermolytic, focal Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma, nonepidermolytic, focal phenotype from the curated OMIM Gene-Disease Associations dataset.

palmoplantar keratoderma, nagashima type Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma, nagashima type phenotype from the curated OMIM Gene-Disease Associations dataset.

keratoderma, palmoplantar, punctate type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratoderma, palmoplantar, punctate type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

keratoderma, palmoplantar, punctate type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratoderma, palmoplantar, punctate type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

keratoderma, palmoplantar, with deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratoderma, palmoplantar, with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

palmoplantar keratoderma, epidermolytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma, epidermolytic phenotype from the curated OMIM Gene-Disease Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

hypertrophic cardiomyopathy and cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

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

cutaneous melanoma which is largely independent of skin type and hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes Gene Set

From HPO Gene-Disease Associations

genes associated with the hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

dilated Gene Set

From GeneRIF Biological Term Annotations

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

dilated fourth ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the dilated fourth ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dilated vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the dilated vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dilated proximal convoluted tubules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated proximal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated distal convoluted tubules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated distal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated endolymphatic duct Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated glomerular capillary Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated glomerular capillary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated lateral ventricles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated lateral ventricles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated lymph node medullary sinus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated lymph node medullary sinus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart atrium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart atrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated bile duct Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated bile duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated pancreatic duct Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated pancreatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated dorsal aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated dorsal aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated sarcoplasmic reticulum Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated sarcoplasmic reticulum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated pharyngeal arch arteries Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated pharyngeal arch arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated gallbladder Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated gallbladder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated pulmonary trunk Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated pulmonary trunk phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated vasculature Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated vasculature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated aorta bulb Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated aorta bulb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated endolymphatic sac Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated endolymphatic sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated renal glomerular capsule Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated renal glomerular capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated kidney calyx Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated kidney calyx phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated third ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated third ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated oviduct Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated oviduct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated seminiferous tubules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated seminiferous tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated terminal bronchiole tubes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated terminal bronchiole tubes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated scala media Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated scala media phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated brunner's glands Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated brunner's glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated rete testis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated rete testis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated basilar artery Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated basilar artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated respiratory conducting tubes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated respiratory conducting tubes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated fourth ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated fourth ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart right ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart right ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated posterior semicircular canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated posterior semicircular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated mitochondria Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated mitochondria phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart left ventricle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart left ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated brain ventricles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated brain ventricles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart right atrium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart right atrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated allantois Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated allantois phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated pulmonary alveolar ducts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated pulmonary alveolar ducts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated seminal vesicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated seminal vesicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated ureter Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated ureter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated esophagus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated esophagus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated aortic sac Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated aortic sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated efferent ductules of testis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated efferent ductules of testis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated uterus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated uterus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated lateral semicircular canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated lateral semicircular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated renal tubules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated renal tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated cochlea Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated cochlea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated uterine cervix Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated uterine cervix phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated kidney collecting duct Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated kidney collecting duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated nephron Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated nephron phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated pulmonary artery Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated pulmonary artery phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated heart left atrium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated heart left atrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated uterine horn Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated uterine horn phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial restrictive cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, restrictive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, restrictive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensorineural deafness with hypertrophic cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensorineural deafness with hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary familial hypertrophic cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, hypertrophic, midventricular, digenic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, hypertrophic, midventricular, digenic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertrophic cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Cardiomyopathy, Restrictive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Restrictive from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Hypertrophic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Alcoholic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Alcoholic from the curated CTD Gene-Disease Associations dataset.

Idiopathic dilation cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Idiopathic dilation cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Hypertrophic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Hypertrophic from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, from the curated CTD Gene-Disease Associations dataset.

Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.

Takotsubo Cardiomyopathy Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.

hypertrophic cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

intrinsic cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

extrinsic cardiomyopathy Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease extrinsic cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

cardiomyopathy Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

restrictive cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

extrinsic cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypertrophic cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peripartum cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcoholic cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intrinsic cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease arrhythmogenic right ventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

chagas cardiomyopathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chagas cardiomyopathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chagas cardiomyopathy; chagas disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chagas cardiomyopathy; chagas disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

desmin-associated restrictive cardiomyopathy. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease desmin-associated restrictive cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, nonfamilial hypertrophic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, nonfamilial hypertrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy; heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy; heart failure; sudden death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy; heart failure; sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tachycardia cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, hypertrophic; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloid cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

stress (tako-tsubo) cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stress (tako-tsubo) cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypertrophic cardiomyopathy. Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, hypertrophic; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chagas cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, hypertrophic, familial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

takotsubo cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, hypertrophic; hepatitis c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy Gene Set

From GeneRIF Biological Term Annotations

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

Cardiomyopathy, Dilated_Myocardial tissue_GSE3586 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Cardiomyopathy, Dilated_Myocardial tissue_GSE3586 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Chagas cardiomyopathy in Tripanosoma cruzi seropositivity Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Chagas cardiomyopathy in Tripanosoma cruzi seropositivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

peripartum cardiomyopathy Gene Set

From GWASdb SNP-Disease Associations

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

hypertrophic cardiomyopathy Gene Set

From GWASdb SNP-Disease Associations

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

intrinsic cardiomyopathy Gene Set

From GWASdb SNP-Disease Associations

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

cardiomyopathy Gene Set

From GWASdb SNP-Disease Associations

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

hypertrophic cardiomyopathy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the hypertrophic cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

cardiomyopathy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

noncompaction cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the noncompaction cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrial cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the atrial cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cardiomyopathy Gene Set

From HPO Gene-Disease Associations

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

right ventricular cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypertrophic cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the hypertrophic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

concentric hypertrophic cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the concentric hypertrophic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

oncocytic cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the oncocytic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cardiomyopathy, Restrictive Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cardiomyopathy, Hypertrophic, Familial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cardiomyopathy, Alcoholic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Chagas Cardiomyopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Chagas Cardiomyopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cardiomyopathy, Hypertrophic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Takotsubo Cardiomyopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Takotsubo Cardiomyopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cardiomyopathy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular cardiomyopathy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

deafness, autosomal dominant 22, with hypertrophic cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, autosomal dominant 22, with hypertrophic cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, early-onset, with fatal cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic, midventricular, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, hypertrophic, midventricular, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) pathway from the Wikipathways Pathways dataset.

ventricular tachycardia; hypertrophic cardiomyopathy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease ventricular tachycardia; hypertrophic cardiomyopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

cardiomyopathy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease cardiomyopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Skin/hair/eye pigmentation, variation in, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Menkes kinky-hair syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Menkes kinky-hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

root hair tip Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the root hair tip cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cell hair Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cell hair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

root hair Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the root hair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Hair Dyes Gene Set

From CTD Gene-Chemical Interactions

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

Menkes Kinky Hair Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Menkes Kinky Hair Syndrome from the curated CTD Gene-Disease Associations dataset.

Hair Diseases Gene Set

From CTD Gene-Disease Associations

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

Cartilage-hair hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE from the curated CTD Gene-Disease Associations dataset.

Hair Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Hair in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Hair Color Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Hair Color in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

hair disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hair follicle neoplasm Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease hair follicle neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

hair disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

hair follicle neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cartilage-hair hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hair disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

black vs red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease black vs red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hair color Gene Set

From GAD Gene-Disease Associations

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

ultrastructure of the hair Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ultrastructure of the hair in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hair thickness Gene Set

From GAD Gene-Disease Associations

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

red vs non-red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red vs non-red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

black vs blond hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease black vs blond hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

straight hair Gene Set

From GAD Gene-Disease Associations

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

blond vs brown hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blond vs brown hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hair morphology Gene Set

From GAD Gene-Disease Associations

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

hair Gene Set

From GAD Gene-Disease Associations

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

hair colour Gene Set

From GAD Gene-Disease Associations

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

hair Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

hair follicle placode formation Gene Set

From GO Biological Process Annotations

genes participating in the hair follicle placode formation biological process from the curated GO Biological Process Annotations dataset.

hair follicle development Gene Set

From GO Biological Process Annotations

genes participating in the hair follicle development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of root hair elongation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of root hair elongation biological process from the curated GO Biological Process Annotations dataset.

regulation of root hair elongation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of root hair elongation biological process from the curated GO Biological Process Annotations dataset.

regulation of hair cycle by canonical wnt signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hair cycle by canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hair cycle Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hair cycle biological process from the curated GO Biological Process Annotations dataset.

regulation of hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

hair cycle phase Gene Set

From GO Biological Process Annotations

genes participating in the hair cycle phase biological process from the curated GO Biological Process Annotations dataset.

hair cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the hair cell differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of hair follicle development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hair follicle development biological process from the curated GO Biological Process Annotations dataset.

establishment of body hair planar orientation Gene Set

From GO Biological Process Annotations

genes participating in the establishment of body hair planar orientation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hair follicle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations dataset.

hair cycle process Gene Set

From GO Biological Process Annotations

genes participating in the hair cycle process biological process from the curated GO Biological Process Annotations dataset.

regulation of hair follicle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hair cycle Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hair cycle biological process from the curated GO Biological Process Annotations dataset.

regulation of hair cycle Gene Set

From GO Biological Process Annotations

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

negative regulation of hair follicle development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hair follicle development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hair follicle development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hair follicle development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

establishment of body hair or bristle planar orientation Gene Set

From GO Biological Process Annotations

genes participating in the establishment of body hair or bristle planar orientation biological process from the curated GO Biological Process Annotations dataset.

hair follicle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the hair follicle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

hair cycle Gene Set

From GO Biological Process Annotations

genes participating in the hair cycle biological process from the curated GO Biological Process Annotations dataset.

hair follicle cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the hair follicle cell proliferation biological process from the curated GO Biological Process Annotations dataset.

hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

Red vs non-red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hair morphology Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hair morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Black vs. red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blond vs. brown hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blond vs. brown hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Black vs. blond hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Black vs. blond hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

hair disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of hair pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

red hair Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the red hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair quantity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hair Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

acquired abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

patchy hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

brittle hair Gene Set

From HPO Gene-Disease Associations

genes associated with the brittle hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of secondary sexual hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse body hair Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse body hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

red hair Gene Set

From HPO Gene-Disease Associations

genes associated with the red hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontal upsweep of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the frontal upsweep of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fair hair Gene Set

From HPO Gene-Disease Associations

genes associated with the fair hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent facial hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent facial hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

projection of scalp hair onto lateral cheek Gene Set

From HPO Gene-Disease Associations

genes associated with the projection of scalp hair onto lateral cheek phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse scalp hair Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse scalp hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature graying of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the premature graying of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pubic hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slow-growing hair Gene Set

From HPO Gene-Disease Associations

genes associated with the slow-growing hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent pubic hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hair growth rate Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of hair growth rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse hair Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hair Gene Set

From HPO Gene-Disease Associations

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

curly hair Gene Set

From HPO Gene-Disease Associations

genes associated with the curly hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

melanin pigment aggregation in hair shafts Gene Set

From HPO Gene-Disease Associations

genes associated with the melanin pigment aggregation in hair shafts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

coarse hair Gene Set

From HPO Gene-Disease Associations

genes associated with the coarse hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hair texture Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of hair texture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scalp hair loss Gene Set

From HPO Gene-Disease Associations

genes associated with the scalp hair loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent axillary hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the scalp hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the scalp hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thick hair Gene Set

From HPO Gene-Disease Associations

genes associated with the thick hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hair pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of hair pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dry hair Gene Set

From HPO Gene-Disease Associations

genes associated with the dry hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse facial hair Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse facial hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair quantity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

extension of hair growth on temples to lateral eyebrow Gene Set

From HPO Gene-Disease Associations

genes associated with the extension of hair growth on temples to lateral eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

silver-gray hair Gene Set

From HPO Gene-Disease Associations

genes associated with the silver-gray hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair laboratory examination Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair whorl Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fine hair Gene Set

From HPO Gene-Disease Associations

genes associated with the fine hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse pubic hair Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large clumps of pigment irregularly distributed along hair shaft Gene Set

From HPO Gene-Disease Associations

genes associated with the large clumps of pigment irregularly distributed along hair shaft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hair-nail ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hair-nail ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the axillary hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hair density Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of hair density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acquired abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

white hair Gene Set

From HPO Gene-Disease Associations

genes associated with the white hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent hair Gene Set

From HPO Gene-Disease Associations

genes associated with the absent hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse axillary hair Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vestibular hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retarded hair growth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retarded hair growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

whorled hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the whorled hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal outer hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brittle hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the brittle hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair medulla air spaces Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal zigzag hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hind foot hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear inner hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle pheomelanosome pheomelanin Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle pheomelanosome pheomelanin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal auchene hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal auchene hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle inner root sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle telogen phase Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear hair bundle ankle links Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair bundle ankle links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear inner hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle melanin granules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair bundle inter-stereocilial links Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair bundle inter-stereocilial links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin hair shaft Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair shaft phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of inner hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair-down neuron morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair-down neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cuticle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cuticle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle dermal papilla morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle dermal papilla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle dermal papilla Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle dermal papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent guard hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent guard hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle infundibulum morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle infundibulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

underdeveloped hair follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the underdeveloped hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

distended hair follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the distended hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased zigzag hair amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased zigzag hair amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle outer root sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle outer root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal outer hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased hair follicle apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased hair follicle apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hair follicle degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal awl hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal awl hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased hair follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of outer hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of outer hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vestibular hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair-down neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair-down neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sparse hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sparse hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick hair follicle outer rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule distribution Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule distribution phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair growth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle matrix region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle matrix region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell synaptic ribbon morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

coarse hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the coarse hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner hair cell kinocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal coat/hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal coat/hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal duvet hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal duvet hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cortex keratinization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cortex keratinization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent awl hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent awl hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle bulge morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle bulge morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair bundle ankle links morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair bundle ankle links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair bundle tip links morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair bundle tip links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle anagen phase Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle anagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear inner hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hair follicle outer rooth sheath hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hair follicle outer rooth sheath hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair medulla Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair medulla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair texture Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair texture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

waved hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the waved hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear inner hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal coat/ hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal coat/ hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal dorsal hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased outer hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal guard hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal guard hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin hair follicle outer rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased inner hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vestibular hair bundle shaft connectors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair bundle shaft connectors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell inter-stereocilial links morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell inter-stereocilial links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle orientation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle orientation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin hair follicle inner rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair follicle inner rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanin granule distribution Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanin granule distribution phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ruffled hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ruffled hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tail hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tail hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cell mechanoelectric transduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cell mechanoelectric transduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the focal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced hair shaft melanin granule number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair bundle shaft connectors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair bundle shaft connectors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle pheomelanosome pheomelanin content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle pheomelanosome pheomelanin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanocyte morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased guard hair length Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased guard hair length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pinna hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pinna hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent active-zone-anchored inner hair cell synaptic ribbon Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair medullary septa cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

progressive hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed hair regrowth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed hair regrowth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged hair follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle catagen phase Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle catagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small hair follicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal guard hair length Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal guard hair length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent duvet hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent duvet hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle regression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle regression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged hair follicle melanin granules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cortex morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased guard hair length Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased guard hair length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of cochlear hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of cochlear hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear outer hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle inner root sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vestibular hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vestibular hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

distorted hair follicle pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

accelerated hair follicle regression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the accelerated hair follicle regression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed hair appearance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed hair appearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shedding Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shedding phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle bulb morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle bulb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

[skin/hair/eye pigmentation 3, blue/green eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 3, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

noonan-like syndrome with loose anagen hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the noonan-like syndrome with loose anagen hair phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation, variation in, 8] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 6, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 6, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 6, blue/green eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 6, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 1, blue/nonblue eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 1, blue/nonblue eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

hair, curly Gene Set

From OMIM Gene-Disease Associations

genes associated with the hair, curly phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 7, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 7, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 5, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 5, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 4, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 4, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, dark/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 9, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 9, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 4, fair/dark skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 8, hair/tooth/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 8, hair/tooth/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, dark/light eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 9, brown/nonbrown eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 9, brown/nonbrown eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

cartilage-hair hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cartilage-hair hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

hair root Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue hair root from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

hair follicle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue hair follicle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

hair Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue hair from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle outer root sheath Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle outer root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair shaft Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair shaft in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle inner root sheath Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle bulge Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle bulge in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair medulla Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

outer hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue outer hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle bulge stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle bulge stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Hair Follicle Development: Induction (Part 1 of 3)(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Hair Follicle Development: Induction (Part 1 of 3)(Homo sapiens) pathway from the Wikipathways Pathways dataset.

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sinoatrial node dysfunction and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From 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.

Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.