congenital disorder of glycosylation type IIl
Disease
congenital disorder of glycosylation type IIl
- Definition
A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG6 gene on chromosome 13q14.11.
- Synonyms
- CDG IIl
- CDG syndrome type IIL
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations
Associated Genes
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