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Congenital disorder of deglycosylation 1
rareA rare autosomal recessive inherited disorder caused by mutations in the NGLY1 gene. It is characterized by developmental delay, hypotonia, abnormal involuntary movements, poor tear production, microcephaly, intractable seizures, abnormal eye movements, and liver abnormalities.
- Identifiers
- MONDO:0800044 OMIM:615273Orphanet:404454
- Causal genes
- NGLY1
- Part of
- Congenital disorder of deglycosylationGlycoprotein metabolism diseaseInborn carbohydrate metabolic disorder
- Also known as
- CDG1V · congenital disorder of glycosylation type IV · congenital disorder of glycosylation, type IV · NGLY1 Deficiency · NGLY1-CDDG
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