Variants
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COG8-CDG

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Description

Syndrome with characteristics of severe psychomotor retardation, failure to thrive and intolerance to wheat and dairy products. So far, only two cases have been described. The disease is caused by mutations in the COG8 gene, which encodes a subunit of the COG complex. This complex is involved vesicle transport in the Golgi apparatus.

SNOMEDCT_US

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

68

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Genes

External Links

  • OMIM

    611182

  • Orphanet

    95428

  • HPO
  • Medgen

    C1970021

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