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Concept information

Preferred term

Amyloid Neuropathies, Familial  

Type

  • Topical Descriptor

Entry terms

  • Amyloidoses, Hereditary Neuropathic
  • Amyloidosis, Hereditary Neuropathic
  • Amyloid Polyneuropathies, Familial
  • Amyloid Polyneuropathy, Familial
  • Familial Amyloid Polyneuropathies
  • Familial Amyloid Polyneuropathy
  • Hereditary Neuropathic Amyloidoses
  • Hereditary Neuropathic Amyloidosis
  • Neuropathic Amyloidoses, Hereditary
  • Neuropathic Amyloidosis, Hereditary
  • Polyneuropathies, Familial Amyloid
  • Polyneuropathy, Familial Amyloid

Scope note

  • Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.

History note

  • 2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001

In other languages

  • Finnish

  • familiaalinen amyloidineuropatia
  • familiaaliset amyloidineuropatiat
  • familiaarinen amyloidineuropatia
  • familiaariset amyloidineuropatiat
  • suvuittainen amyloidineuropatia
  • Swedish

  • Familjär amyloidos med polyneuropati
  • Skelleftesjukan
  • Wohlwill–Corino-Andrades syndrom
  • Ärftlig transtyretinamyloidos

URI

http://www.yso.fi/onto/mesh/D028227

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