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Amyloid Neuropathies, FamilialLegal notice  


Other terms
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,Amyloid Polyneuropathy, Swiss Type,Swiss Type Amyloid Polyneuropathy,Type II Familial Amyloid Polyneuropathy,Familial Amyloid Polyneuropathy, Type II,Familial Amyloid Neuropathy, Portuguese Type,Familial Amyloid Polyneuropathy, Type I,Type I Familial Amyloid Polyneuropathy,Polyneuritic Amyloidosis, Portuguese,Amyloidoses, Portuguese Polyneuritic,Amyloidosis, Portuguese Polyneuritic,Polyneuritic Amyloidoses, Portuguese,Portuguese Polyneuritic Amyloidoses,Portuguese Polyneuritic Amyloidosis,Portuguese Type Familial Amyloid Neuropathy,Familial Amyloid Neuropathy, Andrade Type,Familial Portuguese Polyneuritic Amyloidosis,Familial Amyloid Polyneuropathy, Type VI,Type VI 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,Finnish Type Familial Amyloid Neuropathy,Type V Familial Amyloid Polyneuropathy,Familial Amyloid Neuropathy, Finnish Type,Amyloid Polyneuropathy, British Type,Type III Familial Amyloid Polyneuropathy,Familial Amyloid Polyneuropathy, Type III,Iowa Type Amyloid Polyneuropathy,Amyloid Polyneuropathy, Iowa Type,British Type Amyloid Polyneuropathy,Familial Amyloid Polyneuropathy, Appalachian Type,Appalachian Type Familial Amyloid Polyneuropathy

Description
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.



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