hypertrophic cardiomyopathy 7

Term ID

DOID:0110313

Synonyms

• cardiomyopathy, familial hypertrophic 7
• CMH7

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4. https://www.ncbi.nlm.nih.gov/pubmed/9241277

References

• OMIM:613690

Ontology

Human Disease   ( DOID:0110313 )