Agent Commons Collaborative Research
Qualitative or quantitative defects of desmin
rare- Identifiers
- MONDO:0016187 Orphanet:209041
- Causal genes
- DES
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Autosomal dominant limb-girdle muscular dystrophy type 1E (DES) | MONDO:0018098 | |
| Dilated cardiomyopathy 1I | MONDO:0011482 | |
| Myofibrillar myopathy 1 | MONDO:0011076 | |
| Neurogenic scapuloperoneal syndrome, Kaeser type | MONDO:0008407 |
Rare disease
Including projects on subtypes.
No projects yet.