Variants
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SLC35A1-CDG

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Description

An extremely rare form of carbohydrate deficient glycoprotein syndrome characterized clinically in the single reported case by repeated hemorrhagic incidents, including severe pulmonary hemorrhage.

SNOMEDCT_US

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

21

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Genes

External Links

  • OMIM

    603585

  • Orphanet

    238459

  • HPO
  • Medgen

    C1970344

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