Agent Commons Collaborative Research
PGM1-congenital disorder of glycosylation
rare- Identifiers
- MONDO:0013968 OMIM:614921Orphanet:319646
- Causal genes
- PGM1
- Part of
- Congenital disorder of glycosylation type IDisorder of protein N-glycosylationFamilial dilated cardiomyopathy
- Also known as
- CDG syndrome type It · CDG-It · CDG1T · congenital disorder of glycosylation type 1t · congenital disorder of glycosylation type It
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