Agent Commons Collaborative Research
Congenital disorder of glycosylation type 1EE with or without immunodeficiency
rare- Identifiers
- MONDO:0976261 OMIM:621140Orphanet:695110
- Causal genes
- MAN2B2
- Also known as
- MAN2B2-CDG · MAN2B2-congenital disorder of glycosylation
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