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DOID:0060036 - intrinsic cardiomyopathy
Disease Ontology Definition:A cardiomyopathy that is characterized as weakness in the muscle of the heart that is not due to an identifiable external cause.
Synonyms:
Xenbase Genes : mybpc3, actc1, tnnc1, psen1, myl2, tnnt2, eya4, tpm1, tnni3, tmpo, actn2, jup, dsp, nexn, flnc,
MONDO:0000591 - intrinsic cardiomyopathy |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cardiomyopathy (is_a)