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

Rare disease

Projects

Including projects on subtypes.

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