Ullrich congenital muscular dystrophy
Ullrich congenital muscular dystrophy
Definition
Ullrich congenital muscular dystrophy (UCMD) is characterized by early-onset, generalized and slowly progressive muscle weakness, multiple proximal joint contractures, marked hypermobility of the distal joints and normal intelligence.
Also known as scleroatonic muscular dystrophy, scleroatonic Ullrich disease, UCMD, Ullrich scleroatonic muscular dystrophy — per MONDO
Also identified as
- DOID 0050558 per MONDO
- MESH C537521 per MONDO
- NCIT C123438 per MONDO
- Orphanet 75840 per MONDO
- SCTID 240062007 per MONDO
- UMLS C4551860 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Musculature | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculature | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Peripheral nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Peripheral nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |