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Summary Literature (0)
DOID:0110319 - hypertrophic cardiomyopathy 13

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.

Synonyms: CMH13, cardiomyopathy familial hypertrophic 13,

Xenbase Genes : tnnc1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013195 - hypertrophic cardiomyopathy 13


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypertrophic cardiomyopathy (is_a)