Variants
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Amyotrophic lateral sclerosis type 15

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Description

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene.

MONDO

  • Mode of Inheritance

  • X-linked dominant inheritance

VARIANTS

35

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Genes

External Links

  • OMIM

    300857

  • Orphanet
  • HPO
  • Medgen

    C3275459

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