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MeSH 搜索器

Amyloid Neuropathies, Familial

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.
推出的年份: 2002
副标题
树号: C10.574.500.050, C10.668.829.050.050, C16.320.400.050, C16.320.565.176.050, C18.452.648.176.050, C18.452.845.500.050.050, C18.452.845.500.075.050
MeSH 单一 ID: D028227
进入的组:
  • Amyloid Neuropathy, Familial
  • Familial Amyloid Neuropathies
  • Familial Amyloid Neuropathy
  • Neuropathies, Familial Amyloid
  • Neuropathy, Familial Amyloid
  • Hereditary Neuropathic Amyloidosis
  • Amyloidoses, Hereditary Neuropathic
  • Amyloidosis, Hereditary Neuropathic
  • Hereditary Neuropathic Amyloidoses
  • Neuropathic Amyloidoses, Hereditary
  • Neuropathic Amyloidosis, Hereditary
  • Familial Amyloid Polyneuropathies
  • Amyloid Polyneuropathies, Familial
  • Amyloid Polyneuropathy, Familial
  • Familial Amyloid Polyneuropathy
  • Polyneuropathies, Familial Amyloid
  • Polyneuropathy, Familial Amyloid
  • Familial Amyloid Polyneuropathy, Type VI
  • Type VI Familial Amyloid Polyneuropathy
  • Amyloid Polyneuropathy, British Type
  • British Type Amyloid Polyneuropathy
  • Cerebral Amyloid Angiopathy, British Type
  • Amyloid Polyneuropathy, Iowa Type
  • Iowa Type Amyloid Polyneuropathy
  • Type III Familial Amyloid Polyneuropathy
  • Familial Amyloid Polyneuropathy, Type III
  • Familial Amyloid Neuropathy, Portuguese Type
  • Portuguese Type Familial Amyloid Neuropathy
  • Portuguese Polyneuritic Amyloidosis
  • Amyloidoses, Portuguese Polyneuritic
  • Amyloidosis, Portuguese Polyneuritic
  • Polyneuritic Amyloidoses, Portuguese
  • Portuguese Polyneuritic Amyloidoses
  • Polyneuritic Amyloidosis, Portuguese
  • Wohlwill-Corino Andrade Syndrome
  • Wohlwill Corino Andrade Syndrome
  • Familial Amyloid Neuropathy, Andrade Type
  • Familial Portuguese Polyneuritic Amyloidosis
  • Wohlwill-Andrade Syndrome
  • Wohlwill Andrade Syndrome
  • Amyloid Neuropathy Type 1
  • Neuropathic Amyloid Syndrome
  • Amyloid Syndrome, Neuropathic
  • Amyloid Syndromes, Neuropathic
  • Neuropathic Amyloid Syndromes
  • Type I Familial Amyloid Polyneuropathy
  • Familial Amyloid Polyneuropathy, Type I
  • Familial Amyloid Polyneuropathy, Appalachian Type
  • Appalachian Type Familial Amyloid Polyneuropathy
  • Familial Amyloid Polyneuropathy, Jewish Type
  • Jewish Type Familial Amyloid Polyneuropathy
  • Familial Amyloid Polyneuropathy, Type IV
  • Type IV Familial Amyloid Polyneuropathy
  • Familial Amyloid Polyneuropathy, Type V
  • Familial Amyloid Neuropathy, Finnish Type
  • Finnish Type Familial Amyloid Neuropathy
  • Type V Familial Amyloid Polyneuropathy
  • Amyloid Polyneuropathy, Swiss Type
  • Swiss Type Amyloid Polyneuropathy
  • Type II Familial Amyloid Polyneuropathy
  • Familial Amyloid Polyneuropathy, Type II
早前的内容:
  • Amyloid Neuropathies (1994-2001)
  • Amyloidosis (1967-1993)
  • Peripheral Nervous System Diseases (1967-1993)

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