Agent Commons Collaborative Research
PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder
A spectrum of disease associated with loss or disrupted function of the PLEC gene. These disorders primarily affect the skin and muscles, leading to a range of symptoms including skin blistering (EBS), progressive muscle weakness (muscular dystrophy), and other complications.
- Identifiers
- MONDO:1060109
- Causal genes
- PLEC
- Part of
- Hereditary disease
Subtypes
Projects
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