Passer au contenu principal

Medical Subject Headings (thesaurus)

Choisissez le vocabulaire dans lequel chercher

aligner
annoter
télécharger

Concept information

Nervous System Diseases > Neuromuscular Diseases > Peripheral Nervous System Diseases > Amyloid Neuropathies > Amyloid Neuropathies, Familial
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Proteostasis Deficiencies > Amyloidosis > Amyloid Neuropathies > Amyloid Neuropathies, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System > Amyloid Neuropathies, Familial
Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System > Amyloid Neuropathies, Familial
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Proteostasis Deficiencies > Amyloidosis > Amyloidosis, Familial > Amyloid Neuropathies, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amyloidosis, Familial > Amyloid Neuropathies, Familial
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amyloidosis, Familial > Amyloid Neuropathies, Familial

Terme préférentiel

Amyloid Neuropathies, Familial  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Synonyme(s)

  • Familial Amyloid Polyneuropathies
  • Hereditary Neuropathic Amyloidosis

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-BFPL32GJ-4

Télécharger ce concept :

RDF/XML TURTLE JSON-LD Date de création 25/07/2001, dernière modification le 28/02/2018