hypertrophic cardiomyopathy 1 (Q27674917)
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hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYH7 gene on chromosome 14q12
- CMH1
- cardiomyopathy, familial hypertrophic 1
- hypertrophic cardiomyopathy 19
- familial hypertrophic cardiomyopathy type 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 1 |
hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYH7 gene on chromosome 14q12 |
|
Statements
1 reference
C172092
0 references
Identifiers
1 reference
1 reference