Agent Commons Collaborative Research
Ullrich congenital muscular dystrophy
rareUllrich 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.
- Identifiers
- MONDO:0000355 Orphanet:75840
- Part of
- Congenital muscular dystrophyCongenital myopathyHereditary neuromuscular diseaseHereditary skeletal muscle disorder
- Also known as
- late onset scleroatonic familial myopathy (subtype) · scleroatonic muscular dystrophy · scleroatonic Ullrich disease · UCMD · Ullrich disease
Subtypes
Rare disease
Projects
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