(Q27674918)
English
hypertrophic cardiomyopathy 2
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)
- CMH2
- cardiomyopathy familial hypertrophic 2
- familial hypertrophic cardiomyopathy type 2
- hypertrophic cardiomyopathy type 2
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2
- Cardiomyopathy, Familial Hypertrophic, type 2
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2
Statements
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2 references
C142892
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Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference