hypertrophic cardiomyopathy 3

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Echinobase

Summary

Literature (0)

DOID:0110309 - hypertrophic cardiomyopathy 3

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.

Synonyms: cardiomyopathy familial hypertrophic 3, CMH3

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tpm1

MIM:

MIM:115196 - cardiomyopathy, familial hypertrophic, 3; cmh3

MIM:115196 - cardiomyopathy, familial hypertrophic, 3; cmh3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)