hypertrophic cardiomyopathy 13 (Q27674931)
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hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21
- CMH13
- cardiomyopathy familial hypertrophic 13
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13
- hypertrophic cardiomyopathy type 13
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13
- Cardiomyopathy, Familial Hypertrophic, type 13
- familial hypertrophic cardiomyopathy type 13
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 13 |
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21 |
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