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.

Synonyms: Amyloidosis, Hereditary Neuropathic, Amyloid Polyneuropathy, Familial, Cerebral Amyloid Angiopathy, British Type, Type III Familial Amyloid Polyneuropathy, Amyloid Polyneuropathy, Iowa Type, Familial Amyloid Neuropathy, Portuguese Type, Wohlwill Corino Andrade Syndrome, Polyneuritic Amyloidosis, Portuguese, Amyloid Polyneuropathies, Familial, Neuropathic Amyloidosis, Hereditary, Polyneuritic Amyloidoses, Portuguese, Neuropathic Amyloidoses, Hereditary, Familial Amyloid Neuropathy, Finnish Type, Jewish Type Familial Amyloid Polyneuropathy, Appalachian Type Familial Amyloid Polyneuropathy, Familial Amyloid Polyneuropathy, Type V, Familial Amyloid Neuropathies, Type IV Familial Amyloid Polyneuropathy, Amyloid Neuropathy, Familial, Familial Amyloid Polyneuropathy, Type III, Neuropathic Amyloid Syndrome, Finnish Type Familial Amyloid Neuropathy, Familial Amyloid Polyneuropathy, Type I, Type V Familial Amyloid Polyneuropathy, Amyloid Neuropathy Type 1, Familial Amyloid Neuropathy, Type II Familial Amyloid Polyneuropathy, Familial Amyloid Polyneuropathy, Jewish Type, Wohlwill Andrade Syndrome, Neuropathies, Familial Amyloid, Type I Familial Amyloid Polyneuropathy, Familial Amyloid Neuropathy, Andrade Type, Familial Amyloid Polyneuropathy, Iowa Type Amyloid Polyneuropathy, Portuguese Type Familial Amyloid Neuropathy, Type VI Familial Amyloid Polyneuropathy, Wohlwill-Corino Andrade Syndrome, Amyloidoses, Portuguese Polyneuritic, Amyloid Polyneuropathy, Swiss Type, Familial Amyloid Polyneuropathy, Type IV, Portuguese Polyneuritic Amyloidoses, Hereditary Neuropathic Amyloidoses, Portuguese Polyneuritic Amyloidosis, Familial Amyloid Polyneuropathy, Appalachian Type, Neuropathy, Familial Amyloid, Familial Amyloid Polyneuropathy, Type VI, Amyloid Polyneuropathy, British Type, Familial Amyloid Polyneuropathy, Type II, Swiss Type Amyloid Polyneuropathy, Hereditary Neuropathic Amyloidosis, Familial Portuguese Polyneuritic Amyloidosis, Wohlwill-Andrade Syndrome, Neuropathic Amyloid Syndromes, Polyneuropathy, Familial Amyloid, British Type Amyloid Polyneuropathy, Amyloidosis, Portuguese Polyneuritic, Amyloid Syndromes, Neuropathic, Amyloid Neuropathies, Familial, Familial Amyloid Polyneuropathies, Polyneuropathies, Familial Amyloid, Amyloid Syndrome, Neuropathic, Amyloidoses, Hereditary Neuropathic

Instance information

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2002; see AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES see AMYLOID NEUROPATHIES 1994-2001 ,2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001

identifier

D028227