nemaline myopathy 2 (Q32144835)
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nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23
- NEM2
- nemaline myopathy 2, autosomal recessive
- NEMALINE MYOPATHY 2
- Nemaline Myopathy type 2
- NEMALINE MYOPATHY 2; NEM2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nemaline myopathy 2 |
nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23 |
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C118784
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C118784
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