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DDOST-congenital disorder of glycosylation
rareDDOST-CDG is a form of congenital disorders of N-linked glycosylation characterized by failure to thrive, developmental delay, hypotonia, strabismus and hepatic dysfunction. The disease is caused by mutations in the gene DDOST (1p36.1).
- Identifiers
- MONDO:0013789 OMIM:614507Orphanet:300536
- Causal genes
- DDOST
- Also known as
- carbohydrate deficient glycoprotein syndrome type · carbohydrate deficient glycoprotein syndrome type Ir · CDG syndrome type Ir · CDG-Ir · CDG1R
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