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Summary Literature (0)
DOID:0110308 - hypertrophic cardiomyopathy 2

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2).

Synonyms: cardiomyopathy familial hypertrophic 2, CMH2

Xenbase Genes : tnnt2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007266 - intervertebral disk of atlas

MIM:
MIM:115195 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2

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)