hypertrophic cardiomyopathy 2

Term ID

DOID:0110308

Synonyms

• cardiomyopathy familial hypertrophic 2
• CMH2

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2). https://www.ncbi.nlm.nih.gov/pubmed/8205619

References

• OMIM:115195

Ontology

Human Disease   ( DOID:0110308 )