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DOID:0110309 - hypertrophic cardiomyopathy 3
Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
Synonyms: CMH3, cardiomyopathy familial hypertrophic 3,
Echinobase Genes : tpm1
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):
hypertrophic cardiomyopathy (is_a)