Cardiomyopathy, Hypertrophic, Familial
MeSH code information
- ConceptScope note:An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.
- Tree numbers
Products linked with gene
No products has been found