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DOID:11984 - hypertrophic cardiomyopathy
Disease Ontology Definition:An intrinsic cardiomyopathy that has_material_basis_in autosomal dominant inheritance and that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.
Synonyms: familial hypertrophic cardiomyopathy, hypertrophic obstructive cardiomyopathy,
Echinobase Genes : tpm1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
intrinsic cardiomyopathy (is_a)