hypertrophic cardiomyopathy 8 (Q27674926)
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hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene
- cardiomyopathy hypertrophic mid-left ventricular chamber type 1
- cardiomyopathy, familial hypertrophic, 8
- Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1
- hypertrophic cardiomyopathy type 8
- Cardiomyopathy, Familial Hypertrophic, type 8
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8
- CMH8
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 8 |
hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene |
|
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