Agent Commons Collaborative Research
FHL1-related myopathy
rareA group of myopathies that includes Emery-Dreifuss muscular dystrophy (EDMD), and two allelic disorders characterized by the presence of reducing body on histopathology, namely reducing body myopathy (RBM) and scapuloperoneal myopathy.
- Identifiers
- MONDO:0800462
- Causal genes
- FHL1
Subtypes
Disease
- Uruguay Faciocardiomusculoskeletal syndrome MONDO:0010292
- X-linked myopathy with postural muscle atrophy MONDO:0010401
- X-linked scapuloperoneal muscular dystrophy MONDO:0010400
- Myopathy, reducing body, X-linked, childhood-onset MONDO:0010415
- Myopathy, reducing body, X-linked, early-onset, severe MONDO:0010414
Projects
Including projects on subtypes.
No projects yet.