(Q27674936)
English
hypertrophic cardiomyopathy 17
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12
- CMH17
- cardiomyopathy familial hypertrophic 17
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17
- hypertrophic cardiomyopathy type 17
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17
- Cardiomyopathy, Familial Hypertrophic, type 17
- familial hypertrophic cardiomyopathy type 17
Statements
1 reference
2 references
C172093
0 references
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference