nemaline myopathy 5 (Q32144946)
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nemaline myopathy that has material basis in homozygous mutation in the TNNT1 gene on chromosome 19q13
- nemaline myopathy 5, Amish type
- NEM5
- ANM
- Amish nemaline myopathy
- Nemaline Myopathy, Amish Type
- NEMALINE MYOPATHY 5; NEM5
- NEMALINE MYOPATHY 5
- Nemaline Myopathy type 5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nemaline myopathy 5 |
nemaline myopathy that has material basis in homozygous mutation in the TNNT1 gene on chromosome 19q13 |
|
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