hypertrophic cardiomyopathy 16 (Q27674935)
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hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26
- CMH16
- cardiomyopathy familial hypertrophic 16
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16
- hypertrophic cardiomyopathy type 16
- Cardiomyopathy, Familial Hypertrophic, type 16
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 16 |
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26 |
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