muscular dystrophy-dystroglycanopathy
MONDO:0018276Mondo
Findings
No curated finding names muscular dystrophy-dystroglycanopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Genes
4 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- A kind of
- Narrower terms (7)
- congenital muscular dystrophy with intellectual disability
- congenital muscular dystrophy with intellectual disability and severe epilepsy
- DPM3-congenital disorder of glycosylation
- muscle-eye-brain disease with bilateral multicystic leucodystrophy
- muscular dystrophy-dystroglycanopathy, type A
- muscular dystrophy-dystroglycanopathy, type B
- muscular dystrophy-dystroglycanopathy, type C
Other names
1 name
Resolves to: muscular dystrophy-dystroglycanopathy
- Also called
- CMD due to dystroglycanopathy