Name

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, 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.

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 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, 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.

Tooth agenesis, selective, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tooth agenesis, selective, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tooth agenesis, selective, X-linked, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tooth agenesis, selective, X-linked, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tooth agenesis, selective, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tooth agenesis, selective, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tooth agenesis, selective, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tooth agenesis, selective, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tooth Agenesis, Selective, X-Linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, X-Linked, 1 from the curated CTD Gene-Disease Associations dataset.

Tooth Agenesis, Selective, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, 5 from the curated CTD Gene-Disease Associations dataset.

Tooth Agenesis, Selective, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, 6 from the curated CTD Gene-Disease Associations dataset.

Tooth Agenesis, Selective, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, 3 from the curated CTD Gene-Disease Associations dataset.

Tooth Agenesis, Selective, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tooth Agenesis, Selective, 2 from the curated CTD Gene-Disease Associations dataset.

tooth agenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Tooth agenesis (third molar) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Tooth agenesis (third molar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

tooth agenesis Gene Set

From GWASdb SNP-Disease Associations

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

selective tooth agenesis Gene Set

From GWASdb SNP-Phenotype Associations

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

selective tooth agenesis Gene Set

From HPO Gene-Disease Associations

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

tooth agenesis, selective, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 1, with or without orofacial cleft Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.

Primary tooth development (time to first tooth eruption) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Primary tooth development (time to first tooth eruption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype 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.

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 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.

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 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.

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.

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.

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.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital with inner ear agenesis, microtia, and microdontia Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital with inner ear agenesis, microtia, and microdontia phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic and cerebellar agenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic and cerebellar agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations 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.

tooth and nail syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gingival crevicular fluid and orthodontic tooth movement Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival crevicular fluid and orthodontic tooth movement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Sacral agenesis with vertebral anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sacral agenesis with vertebral anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus, permanent neonatal, with cerebellar agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary renal agenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary renal agenesis from the curated CTD Gene-Disease Associations dataset.

Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Partial Agenesis of, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Partial Agenesis of, X-Linked from the curated CTD Gene-Disease Associations dataset.

Pancreatic beta cell agenesis with neonatal diabetes mellitus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pancreatic beta cell agenesis with neonatal diabetes mellitus from the curated CTD Gene-Disease Associations dataset.

Corpus callosum agenesis neuronopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus callosum agenesis neuronopathy from the curated CTD Gene-Disease Associations dataset.

Pancreatic Agenesis, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pancreatic Agenesis, Congenital from the curated CTD Gene-Disease Associations dataset.

renal agenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

agenesis of the corpus callosum Gene Set

From GAD Gene-Disease Associations

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

hypothyroidism; cleft palate, isolated; thyroid agenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypothyroidism; cleft palate, isolated; thyroid agenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

agenesis Gene Set

From GeneRIF Biological Term Annotations

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

agenesis of pineal gland Gene Set

From HPO Gene-Disease Associations

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

partial agenesis of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the partial agenesis of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

agenesis of cerebellar vermis Gene Set

From HPO Gene-Disease Associations

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

parathyroid agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of maxillary lateral incisor Gene Set

From HPO Gene-Disease Associations

genes associated with the agenesis of maxillary lateral incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

partial abdominal muscle agenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the partial abdominal muscle agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of permanent teeth Gene Set

From HPO Gene-Disease Associations

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

adrenal gland agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of maxillary incisor Gene Set

From HPO Gene-Disease Associations

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

olfactory lobe agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of central incisor Gene Set

From HPO Gene-Disease Associations

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

agenesis of corpus callosum Gene Set

From HPO Gene-Disease Associations

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

agenesis of lateral incisor Gene Set

From HPO Gene-Disease Associations

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

unilateral renal agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of mandibular central incisor Gene Set

From HPO Gene-Disease Associations

genes associated with the agenesis of mandibular central incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

agenesis of incisor Gene Set

From HPO Gene-Disease Associations

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

bilateral lung agenesis Gene Set

From HPO Gene-Disease Associations

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

thyroid agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of pulmonary vessels Gene Set

From HPO Gene-Disease Associations

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

agenesis of mandibular incisor Gene Set

From HPO Gene-Disease Associations

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

anterior pituitary agenesis Gene Set

From HPO Gene-Disease Associations

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

agenesis of the diaphragm Gene Set

From HPO Gene-Disease Associations

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

renal agenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

agenesis of the corpus callosum with peripheral neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corpus callosum, partial agenesis of Gene Set

From OMIM Gene-Disease Associations

genes associated with the corpus callosum, partial agenesis of phenotype from the curated OMIM Gene-Disease Associations dataset.

sacral agenesis with vertebral anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the sacral agenesis with vertebral anomalies 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.

Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IVF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Failure of tooth eruption, primary Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Failure of tooth eruption, primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease dominant intermediate 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate d Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate c Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, Type 2K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1D from the curated CTD Gene-Disease Associations dataset.

Tooth Abnormalities Gene Set

From CTD Gene-Disease Associations

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

Charcot-Marie-Tooth disease, X-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset.

Tooth Loss Gene Set

From CTD Gene-Disease Associations

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

Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1e from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Type 4j Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4j from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4C from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4E from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Recessive Intermediate A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Recessive Intermediate A from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1F from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2G from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2D from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2E from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2I from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2F from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2J from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2H from the curated CTD Gene-Disease Associations dataset.

Failure of Tooth Eruption, Primary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Failure of Tooth Eruption, Primary from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Type 4H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.

Tooth Injuries Gene Set

From CTD Gene-Disease Associations

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

Charcot-Marie-Tooth disease, Type 2B1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2B2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B2 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4B1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4B2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B2 from the curated CTD Gene-Disease Associations dataset.

Tooth Eruption Gene Set

From dbGAP Gene-Trait Associations

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

tooth disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

charcot-marie-tooth disease type 3 Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease charcot-marie-tooth disease type 3 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

charcot-marie-tooth disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

tooth disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

tooth disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tooth ankylosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

charcot-marie-tooth disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tooth erosion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

charcot-marie-tooth disease type x Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease charcot-marie-tooth disease type x in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

charcot-marie-tooth disease type 4 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease charcot-marie-tooth disease type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

charcot-marie-tooth disease type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease charcot-marie-tooth disease type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

charcot-marie-tooth disease type 3 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease charcot-marie-tooth disease type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

charcot-marie-tooth disease type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease charcot-marie-tooth disease type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

tooth resorption Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tooth loss Gene Set

From GAD Gene-Disease Associations

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

clinically distinct charcot-marie-tooth phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease clinically distinct charcot-marie-tooth phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy type 1b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth neuropathy type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mouth, edentulous; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mouth, edentulous; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autosomal recessive charcot-marie-tooth disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autosomal recessive charcot-marie-tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anodontia; developmental absence of tooth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anodontia; developmental absence of tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuropathy, charcot-marie-tooth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuropathy, charcot-marie-tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary tooth development Gene Set

From GAD Gene-Disease Associations

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

recessive charcot-marie-tooth disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth type 1b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease Gene Set

From GAD Gene-Disease Associations

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

x-linked charcot-marie tooth disease Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; periodontal attachment loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; genetic diseases, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; genetic diseases, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periodontal attachment loss; periodontitis; tooth mobility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth type 1 disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth type 1 disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease type 1a Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease type 1a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease type 1b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; tooth abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; tooth abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tooth eruption Gene Set

From GAD Gene-Disease Associations

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

tooth Gene Set

From GeneRIF Biological Term Annotations

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

positive regulation of tooth mineralization Gene Set

From GO Biological Process Annotations

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

negative regulation of tooth mineralization Gene Set

From GO Biological Process Annotations

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

negative regulation of odontogenesis of dentin-containing tooth Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations dataset.

tooth mineralization Gene Set

From GO Biological Process Annotations

genes participating in the tooth mineralization biological process from the curated GO Biological Process Annotations dataset.

positive regulation of odontogenesis of dentin-containing tooth Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations dataset.

odontogenesis of dentin-containing tooth Gene Set

From GO Biological Process Annotations

genes participating in the odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations dataset.

regulation of tooth mineralization Gene Set

From GO Biological Process Annotations

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

tooth eruption Gene Set

From GO Biological Process Annotations

genes participating in the tooth eruption biological process from the curated GO Biological Process Annotations dataset.

regulation of odontogenesis of dentin-containing tooth Gene Set

From GO Biological Process Annotations

genes participating in the regulation of odontogenesis of dentin-containing tooth biological process from the curated GO Biological Process Annotations dataset.

structural constituent of tooth enamel Gene Set

From GO Molecular Function Annotations

genes performing the structural constituent of tooth enamel molecular function from the curated GO Molecular Function Annotations dataset.

Primary tooth development (number of teeth) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Primary tooth development (number of teeth) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Permanent tooth development Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Permanent tooth development phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

tooth disease Gene Set

From GWASdb SNP-Disease Associations

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

unerupted tooth Gene Set

From HPO Gene-Disease Associations

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

natal tooth Gene Set

From HPO Gene-Disease Associations

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

molar tooth sign on mri Gene Set

From HPO Gene-Disease Associations

genes associated with the molar tooth sign on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

double tooth Gene Set

From HPO Gene-Disease Associations

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

impacted tooth Gene Set

From HPO Gene-Disease Associations

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

conical tooth Gene Set

From HPO Gene-Disease Associations

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

Tooth Abnormalities Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth Demineralization Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth, Supernumerary Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth, Nonvital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth Mobility Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Charcot-Marie-Tooth Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal tooth morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent tooth primordium Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tooth mineralization Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tooth hard tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tooth hard tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

embryonic lethality prior to tooth bud stage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the embryonic lethality prior to tooth bud stage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

arrest of tooth development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the arrest of tooth development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tooth eruption Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tooth root development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tooth development Gene Set

From MPO Gene-Phenotype Associations

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

delayed tooth eruption Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tooth color Gene Set

From MPO Gene-Phenotype Associations

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

failure of tooth eruption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of tooth eruption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

accelerated tooth eruption Gene Set

From MPO Gene-Phenotype Associations

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

charcot-marie-tooth disease, dominant intermediate f Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, dominant intermediate f phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, dominant intermediate e Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, dominant intermediate e phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, dominant intermediate d Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, dominant intermediate d phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, dominant intermediate c Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, dominant intermediate c phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, dominant intermediate b Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, dominant intermediate b phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, dominant intermediate a Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, dominant intermediate a phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, type 2r Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, x-linked dominant, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, x-linked dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, x-linked recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, x-linked recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, recessive intermediate, a Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, recessive intermediate, a phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2a1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2a1 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2a2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2a2 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, foot deformity of Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, foot deformity of phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 1c Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 1c phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

failure of tooth eruption, primary Gene Set

From OMIM Gene-Disease Associations

genes associated with the failure of tooth eruption, primary phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, recessive intermediate d Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, recessive intermediate d phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, recessive intermediate c Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, recessive intermediate c phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, type 4b3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, type 4b3 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4b2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4b2 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4b1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4b1 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, recessive intermediate, b Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, recessive intermediate, b phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2s Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2k Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2k phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2n Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2n phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2m Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2m phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2g Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2f Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2b1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2b1 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2b2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2b2 phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2j Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 2i Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 2i phenotype from the curated OMIM Gene-Disease Associations dataset.

?charcot-marie-tooth disease, axonal, type 2q Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?charcot-marie-tooth disease, axonal, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4h Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4h phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4j Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4j phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4c Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4c phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4d Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4d phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, type 4f Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, type 4f phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, with vocal cord paresis Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, with vocal cord paresis phenotype from the curated OMIM Gene-Disease Associations dataset.

charcot-marie-tooth disease, axonal, type 2l Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, axonal, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth bud Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue tooth bud from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

tooth Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue tooth from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

tooth enamel Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue tooth enamel in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

tooth Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue tooth in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

tooth bud Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue tooth bud in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

tooth germ Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue tooth germ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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 r