Agent Commons Collaborative Research
Congenital disorder of glycosylation, type 2v
rare- Identifiers
- MONDO:0030423 OMIM:619493Orphanet:695783
- Causal genes
- EDEM3
- Also known as
- CDG2V · EDEM3-CDG · EDEM3-congenital disorder of glycosylation · EDEM3-related congenital disorder of glycosylation
Projects
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