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Summary Literature (0)
DOID:0110318 - hypertrophic cardiomyopathy 12

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.

Synonyms: cardiomyopathy familial hypertrophic 12, CMH12

Xenbase Genes : csrp3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012804 - hypertrophic cardiomyopathy 12


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)