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Concept information

disease > metabolic diseases > familial amyloidotic polyneuropathy type 1
disease > nervous system diseases > familial amyloidotic polyneuropathy type 1
disease > nervous system diseases > peripheral nerve disease > polyneuropathy > familial amyloidotic polyneuropathy type 1

Terme préférentiel

familial amyloidotic polyneuropathy type 1  

Définition

  • Familial amyloid polyneuropathy, also called transthyretin-related hereditary amyloidosis, transthyretin amyloidosis abbreviated also as ATTR (hereditary form), or Corino de Andrade's disease, is an autosomal dominant neurodegenerative disease (Wikipedia)

Concept générique

Synonyme(s)

  • amyloid neuropathy type I
  • Andrade's paramyeloidosis
  • Andrade's type of heritable polyneuropathy
  • British type amyloidosis
  • Corino de Andrade syndrome
  • familial Portuguese polyneuritic amyloidosis
  • hereditary neuropathic amyloidosis
  • Japanese type amyloidosis
  • neuropathic amyloid syndrome
  • neuropathic hereditary amyloidosis
  • Portuguese type of hereditary neuropathic amyloidosis
  • Swedish type amyloidosis
  • transhyretin abnormality
  • TTR abnormality
  • Wohlwill-Corino Andrade syndrome

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-NNL526RR-H

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