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Summary Literature (0)
DOID:0110313 - hypertrophic cardiomyopathy 7

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.

Synonyms: cardiomyopathy, familial hypertrophic 7, CMH7

Xenbase Genes : tnni3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013369 - hypertrophic cardiomyopathy 7


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)