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Inborn genetic diseases

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Description

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.

MSH

  • Mode of Inheritance

    VARIANTS

    4,156

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    Genes

      External Links

      • OMIM
      • Orphanet
      • HPO
      • Medgen

        C0950123

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