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Autosomal dominant Parkinson disease 4

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Description

A late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

0

Genes

External Links

  • OMIM

    605543

  • Orphanet
  • HPO
  • Medgen

    C1854182

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