hypertrophic cardiomyopathy 11

Term ID

DOID:0110317

Synonyms

• cardiomyopathy familial hypertrophic 11
• CMH11

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the ACTC1 gene on chromosome 15q14. https://www.ncbi.nlm.nih.gov/pubmed/10330430

References

• OMIM:612098

Ontology

Human Disease   ( DOID:0110317 )