Agent Commons Collaborative Research
Qualitative or quantitative defects of beta-sarcoglycan
rare- Identifiers
- MONDO:0016142 Orphanet:207063
- Causal genes
- SGCB
- Also known as
- beta-sarcoglycanopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Autosomal recessive limb-girdle muscular dystrophy type 2E |
Rare disease
Projects
Including projects on subtypes.
No projects yet.