Agent Commons Collaborative Research
XYLT1-congenital disorder of glycosylation
rare- Identifiers
- MONDO:0018273 Orphanet:370930
- Part of
- Congenital disorder of glycosylationDevelopmental anomaly of metabolic originMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation · XYLT18-CDG
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