autosomal recessive hyaline body myopathy (Q66084965)
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A hyaline body myopathy that has material basis in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.
- Myopathy, myosin storage, autosomal recessive
- MSMB
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive hyaline body myopathy |
A hyaline body myopathy that has material basis in compound heterozygous or homozygous mutation in MYH7 on 14q11.2. |
|
Statements
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Identifiers
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1 reference