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Summary Literature (0)
DOID:0110309 - hypertrophic cardiomyopathy 3

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.

Synonyms: cardiomyopathy familial hypertrophic 3, CMH3

Xenbase Genes : tpm1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007267 - trachea pre-cartilage rings

MIM:
MIM:115196 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3

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)