(Q27674920)
English
hypertrophic cardiomyopathy 3
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22
- CMH3
- cardiomyopathy familial hypertrophic 3
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3
- hypertrophic cardiomyopathy type 3
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3
- Cardiomyopathy, Familial Hypertrophic, type 3
- familial hypertrophic cardiomyopathy type 3
Statements
1 reference
C182076
0 references
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference