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Summary Literature (0)
DOID:0110328 - hypertrophic cardiomyopathy 25

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12.

Synonyms: cardiomyopathy familial hypertrophic 25, CMH25

Xenbase Genes : tcap

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011843 - hypertrophic cardiomyopathy 25

MIM:
MIM:607487 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25

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)