Agent Commons Collaborative Research
Muscular dystrophy-dystroglycanopathy
rare- Identifiers
- MONDO:0018276 Orphanet:370953
- Part of
- Congenital muscular dystrophy
- Also known as
- CMD due to dystroglycanopathy
Subtypes
Disease Rare Not rare Subtypes
- Muscular dystrophy-dystroglycanopathy, type A MONDO:0000171 14
- Muscular dystrophy-dystroglycanopathy, type C MONDO:0000173 10
- Muscular dystrophy-dystroglycanopathy, type B MONDO:0000172 8
- DPM3-congenital disorder of glycosylation MONDO:0013049 DPM3 1
- Congenital muscular dystrophy with intellectual disability MONDO:0018278
- Congenital muscular dystrophy with intellectual disability and severe epilepsy MONDO:0014023 DPM2
- Muscle-eye-brain disease with bilateral multicystic leucodystrophy MONDO:0018280
Projects
Including projects on subtypes.
No projects yet.