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Hemoglobinopathy

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Description

An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.

NCI

  • Mode of Inheritance

    VARIANTS

    28

    SEE THE VARIANTS →

    Genes

    • HBA1
    • HBA2
    • HBB

    • HBB-LCR

    External Links

    • OMIM
    • Orphanet
    • HPO
    • Medgen

      C0019045

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