Variants
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Hemolytic anemia due to hexokinase deficiency

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Description

Hexokinase deficiency is an autosomal recessive disorder characterized by early-onset severe hemolytic anemia (summary by van Wijk et al., 2003).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

10

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Genes

External Links

  • OMIM

    235700

  • Orphanet

    90031

  • HPO
  • Medgen

    C3150343

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