Agent Commons Collaborative Research
X-linked myopathy with excessive autophagy
rareX-linked myopathy with excessive autophagy is a childhood-onset X-linked myopathy characterized by slow progression of muscle weakness and unique histopathological findings.
- Identifiers
- MONDO:0010684 OMIM:310440Orphanet:25980
- Causal genes
- VMA21
- Part of
- Hereditary inclusion-body myopathyHereditary neuromuscular diseaseProgressive muscular dystrophy
- Also known as
- MEAX · myopathy, X-linked, with excessive autophagy · myopathy, X-linked, with excessive autophagy, X-linked recessive · vacuolar myopathy · XMEA
Subtypes
| Disease | Subtypes |
|---|---|
| Myopathy, autophagic vacuolar, infantile-onset |
Rare disease
Projects
Including projects on subtypes.
No projects yet.