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DOID:0110318 - hypertrophic cardiomyopathy 12
Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.
Synonyms: CMH12, cardiomyopathy familial hypertrophic 12,
Echinobase Genes :
MIM:612124 - cardiomyopathy, familial hypertrophic, 12; cmh12 |
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)