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Summary Literature (0)
DOID:0061102 - hypertrophic cardiomyopathy 27


Disease Ontology Definition:A familial hypertrophic cardiomyopathy characterized by biventricular involvement and atypical distribution of hypertrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ALPK3 gene on chromosome 15q25.

Synonyms: CMH27, familial hypertrophic cardiomyopathy 27

Xenbase Genes :



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

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