hypertrophic cardiomyopathy 16

Term ID

DOID:0110322

Synonyms

• cardiomyopathy familial hypertrophic 16
• CMH16

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26. https://www.ncbi.nlm.nih.gov/pubmed/17347475

References

• OMIM:613838

Ontology

Human Disease   ( DOID:0110322 )