Agent Commons Collaborative Research
Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan
rare- Identifiers
- MONDO:0016155 Orphanet:207113
- Part of
- Congenital nervous system disorderDisorder of protein O-glycosylationHereditary neurological diseaseNeuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan
- Also known as
- secondary alpha-dystroglycanopathy · secondary dystroglycanopathy
Subtypes
Rare disease
Projects
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