Amyloid Neuropathies,Familial

《英文msh詞典》Amyloid Neuropathies,Familial
[主題詞] Amyloid Neuropathies,Familial
[同義詞] Familial Amyloid Polyneuropathies
[入口詞] Amyloid Polyneuropathy,British Type
[入口詞] Amyloid Polyneuropathy,Iowa Type
[入口詞] Amyloid Polyneuropathy,Swiss Type
[入口詞] Appalachian Type Familial Amyloid Polyneuropathy
[入口詞] British Type Amyloid Polyneuropathy
[入口詞] Familial Amyloid Neuropathy,Andrade Type
[入口詞] Familial Amyloid Neuropathy,Finnish Type
[入口詞] Familial Amyloid Neuropathy,Portuguese Type
[入口詞] Familial Amyloid Polyneuropathy,Appalachian Type
[入口詞] Familial Amyloid Polyneuropathy,Jewish Type
[入口詞] Familial Amyloid Polyneuropathy,Type I
[入口詞] Familial Amyloid Polyneuropathy,Type II
[入口詞] Familial Amyloid Polyneuropathy,Type III
[入口詞] Familial Amyloid Polyneuropathy,Type IV
[入口詞] Familial Amyloid Polyneuropathy,Type V
[入口詞] Familial Amyloid Polyneuropathy,Type VI
[入口詞] Finnish Type Familial Amyloid Neuropathy
[入口詞] Iowa Type Amyloid Polyneuropathy
[入口詞] Jewish Type Familial Amyloid Polyneuropathy
[入口詞] Polyneuritic Amyloidosis,Portuguese
[入口詞] Portuguese Polyneuritic Amyloidosis
[入口詞] Portuguese Type Familial Amyloid Neuropathy
[入口詞] Swiss Type Amyloid Polyneuropathy
[入口詞] Type I Familial Amyloid Polyneuropathy
[入口詞] Type II Familial Amyloid Polyneuropathy
[入口詞] Type III Familial Amyloid Polyneuropathy
[入口詞] Type IV Familial Amyloid Polyneuropathy
[入口詞] Type V Familial Amyloid Polyneuropathy
[入口詞] Type VI Familial Amyloid Polyneuropathy
[入口詞] Amyloid Neuropathy,Familial
[入口詞] Amyloid Polyneuropathies,Familial
[入口詞] Amyloid Polyneuropathy,Familial
[入口詞] Amyloidoses,Portuguese Polyneuritic
[入口詞] Amyloidosis,Portuguese Polyneuritic
[入口詞] Familial Amyloid Neuropathies
[入口詞] Familial Amyloid Neuropathy
[入口詞] Familial Amyloid Polyneuropathy
[入口詞] Neuropathies,Familial Amyloid
[入口詞] Neuropathy,Familial Amyloid
[入口詞] Polyneuritic Amyloidoses,Portuguese
[入口詞] Polyneuropathies,Familial Amyloid
[入口詞] Polyneuropathy,Familial Amyloid
[入口詞] Portuguese Polyneuritic Amyloidoses
[中文釋義] 淀粉樣神經病,家族性
[英文釋義] 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.