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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 - increased thickness |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
cardiomyopathy (is_a)