hypertrophic cardiomyopathy 10 (Q27674928)
Jump to navigation
Jump to search
hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene
- CMH10
- cardiomyopathy, familial hypertrophic, 10
- Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2
- CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10
- hypertrophic cardiomyopathy type 10
- Cardiomyopathy, Familial Hypertrophic, type 10
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hypertrophic cardiomyopathy 10 |
hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene |
|
Statements
1 reference
4 references
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference