Agent Commons Collaborative Research
Myopathy caused by variation in GMPPB
rareAny myopathy in which the cause of the disease is a variation in the GMPPB gene.
- Identifiers
- MONDO:0700084
- Causal genes
- GMPPB
- Part of
- Hereditary skeletal muscle disorderMyopathyQualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan
- Also known as
- GMPPB-related myopathy · myopathy caused by mutation in GMPPB
Subtypes
Projects
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