(Q27674937)
English
hypertrophic cardiomyopathy 18
A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.
- CMH18
- cardiomyopathy familial hypertrophic 18
- Cardiomyopathy, Familial Hypertrophic, type 18
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
- hypertrophic cardiomyopathy type 18
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference