Agent Commons Collaborative Research
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
rare- Identifiers
- MONDO:0029135 OMIM:618135
- Part of
- Autosomal recessive limb-girdle muscular dystrophyCongenital muscular dystrophy caused by variation in POMGNT2Muscular dystrophy-dystroglycanopathy, type C
- Also known as
- LGMD-POMGNT2 related myopathy · MDDGC8
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