hypertrophic cardiomyopathy 20

Term ID

DOID:0110326

Synonyms

• cardiomyopathy familial hypertrophic 20
• CMH20

Definition

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1. https://www.ncbi.nlm.nih.gov/pubmed/20970104

References

• OMIM:613876

Ontology

Human Disease   ( DOID:0110326 )