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DOID:11984 - hypertrophic cardiomyopathy
Disease Ontology Definition:An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.
Synonyms: familial hypertrophic cardiomyopathy, hypertrophic obstructive cardiomyopathy
Xenbase Genes
:
mybpc3,
actc1,
tnnc1,
myl2,
tnnt2,
tpm1,
tnni3,
nexn,
flnc,
myoz2,
prkag2,
myl3,
cav3,
jph2,
myh6,
| MONDO:0005045 - mucosa of ethmoidal sinus |
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)