Variants
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HNSHA due to aldolase A deficiency

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Description

Aldolase A deficiency is an autosomal recessive disorder associated with hereditary hemolytic anemia (Kishi et al., 1987).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

47

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Genes

External Links

  • OMIM

    611881

  • Orphanet

    57

  • HPO
  • Medgen

    C0272066

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