(Q27674939)
English
hypertrophic cardiomyopathy 20
A hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
- CMH20
- cardiomyopathy familial hypertrophic 20
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20
- hypertrophic cardiomyopathy type 20
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20
- Cardiomyopathy, Familial Hypertrophic, type 20
Statements
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Identifiers
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