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Summary Literature (0)
DOID:0110324 - hypertrophic cardiomyopathy 18

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.

Synonyms: cardiomyopathy familial hypertrophic 18, CMH18

Xenbase Genes : pln

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013475 - hypertrophic cardiomyopathy 18


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)