autosomal dominant hyaline body myopathy (Q66084966)
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A hyaline body myopathy that has material basis in heterozygous mutation in MYH7 on 14q11.2.
- MSMA
- myopathy with lysis of type I myofibrils
- Myopathy, myosin storage, autosomal dominant
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant hyaline body myopathy |
A hyaline body myopathy that has material basis in heterozygous mutation in MYH7 on 14q11.2. |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference