hypertrophic cardiomyopathy 10

Term ID

DOID:0110316

Synonyms

• cardiomyopathy, familial hypertrophic, 10
• CMH10

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene. https://www.ncbi.nlm.nih.gov/pubmed/8673105

References

• OMIM:608758

Ontology

Human Disease   ( DOID:0110316 )