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Insomnia, Fatal Familial

An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).

Year introduced: 2003

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Subheadings:

Tree Number(s): C01.207.800.392, C10.228.228.800.392, C10.574.843.512, C10.886.425.800.800.400

MeSH Unique ID: D034062

Entry Terms:

  • Fatal Familial Insomnias
  • Insomnias, Fatal Familial
  • Fatal Familial Insomnia
  • Insomnia Familial Fatal
  • Familial Fatal, Insomnia
  • Familial Fatals, Insomnia
  • Fatal, Insomnia Familial
  • Fatals, Insomnia Familial
  • Insomnia Familial Fatals
  • Familial Fatal Insomnia
  • Familial Fatal Insomnias
  • Fatal Insomnia, Familial
  • Fatal Insomnias, Familial
  • Insomnia, Familial Fatal
  • Insomnias, Familial Fatal

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