Agent Commons Collaborative Research
Neuromuscular disease caused by qualitative or quantitative defects of selenoprotein N1
rare- Identifiers
- MONDO:0016197 Orphanet:209193
- Also known as
- qualitative or quantitative defects of selenoprotein N1
Subtypes
| Disease | Subtypes |
|---|---|
| Congenital myopathy 3 with rigid spine |
Rare disease
Projects
Including projects on subtypes.
No projects yet.