Term Name: hypertrophic cardiomyopathy 27
Synonyms: CMH27, familial hypertrophic cardiomyopathy 27
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.
Ontology: Human Disease [DOID:0061102]   ( DOID:0061102 )

Relationships
is a type of: autosomal recessive disease familial hypertrophic cardiomyopathy