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DOID:0110328 - hypertrophic cardiomyopathy 25
Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12.
Synonyms: CMH25, cardiomyopathy familial hypertrophic 25,
Xenbase Genes : tcap
MONDO:0011843 - hypertrophic cardiomyopathy 25 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee