Agent Commons Collaborative Research
COG6-congenital disorder of glycosylation
rare- Identifiers
- MONDO:0013810 OMIM:614576Orphanet:464443
- Causal genes
- COG6
- Also known as
- CDG syndrome type IIL · CDG-IIL · CDG2L · CDGIIl · COG6-CDG
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