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DOID:0110319 - hypertrophic cardiomyopathy 13
Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.
Synonyms: CMH13, cardiomyopathy familial hypertrophic 13,
Echinobase Genes :
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)