Term Name:	hypertrophic cardiomyopathy 18
Synonyms:	cardiomyopathy familial hypertrophic 18, CMH18
Definition:	A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
Ontology:	Human Disease [DOID:0110324]   ( DOID:0110324 )