hypertrophic cardiomyopathy 12

Term ID

DOID:0110318

Synonyms

• cardiomyopathy familial hypertrophic 12
• CMH12

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/12642359

References

• OMIM:612124

Ontology

Human Disease   ( DOID:0110318 )