NIH GARD Information: Limb-girdle muscular dystrophy type 2O
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3
- MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED
- Autosomal recessive limb-girdle muscular dystrophy type 2O
- POMGNT1-related limb-girdle muscular dystrophy R15
- LGMD type 2O
- POMGNT1-related LGMD R15
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.