Variants
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ALG9 congenital disorder of glycosylation

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Description

Congenital disorders of glycosylation (CDGs) that represent defects of dolichol-linked oligosaccharide assembly are classified as CDG type I. For a general description and a discussion of the classification of CDGs, see CDG1A (212065).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

182

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Genes

External Links

  • OMIM

    608776

  • Orphanet

    79328

  • HPO
  • Medgen

    C2931006

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