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Summary Literature (0)
DOID:0110325 - hypertrophic cardiomyopathy 19

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the calreticulin gene (CALR3) on chromosome 19p13.11.

Synonyms: CMH19, cardiomyopathy familial hypertrophic 19,

Xenbase Genes : calr3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013476 - hypertrophic cardiomyopathy 19


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)