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Echinobase
Summary Literature (0)
DOID:0110323 - hypertrophic cardiomyopathy 17

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12.

Synonyms: CMH17, cardiomyopathy familial hypertrophic 17,

Echinobase Genes :


OMIM:
MIM:613873 - cardiomyopathy, familial hypertrophic, 17; cmh17

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypertrophic cardiomyopathy (is_a)