hypertrophic cardiomyopathy 27

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.

Also known as: CMH27; familial hypertrophic cardiomyopathy 27