(Q27674926)
English
hypertrophic cardiomyopathy 8
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
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Identifiers
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