The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Amyloid Neuropathies, Familial
Hierarchy: | ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial 27 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial ∟ ∟ ∟ ∟ ∟ Amyloid Neuropathies, Familial |
History note: | Amyloid Neuropathies (1994-2001) | Amyloidosis (1967-1993) | Peripheral Nervous System Diseases (1967-1993)X |
historyNote*: | 2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001
X |
publicMeSHNote*: | 2002; see AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES see AMYLOID NEUROPATHIES 1994-2001
X |
Scope note: | 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.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 2001-07-25X |
dateEstablished*: | 2002-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | nnsX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Suvuittaiset amyloidineuropatit (fi) XSuvuittainen amyloidineuropatia (fi, replaced) Familiaaliset amyloidineuropatiat (fi, replaced) Familiaalinen amyloidineuropatia (fi, replaced) Amyloidneuropatier, familjära (sv) Type II Familial Amyloid Polyneuropathy (en, replaced) Type III Familial Amyloid Polyneuropathy (en, replaced) Type I Familial Amyloid Polyneuropathy (en, replaced) Swiss Type Amyloid Polyneuropathy (en, replaced) Portuguese Type Familial Amyloid Neuropathy (en, replaced) Type IV Familial Amyloid Polyneuropathy (en, replaced) Type V Familial Amyloid Polyneuropathy (en, replaced) Type VI Familial Amyloid Polyneuropathy (en, replaced) Portuguese Polyneuritic Amyloidosis (en, replaced) Polyneuritic Amyloidosis, Portuguese (en, replaced) Familial Amyloid Polyneuropathies (en, replaced) Familial Amyloid Neuropathy, Andrade Type (en, replaced) British Type Amyloid Polyneuropathy (en, replaced) Appalachian Type Familial Amyloid Polyneuropathy (en, replaced) Familial Amyloid Polyneuropathy, Type I (en, replaced) Familial Amyloid Polyneuropathy, Type II (en, replaced) Jewish Type Familial Amyloid Polyneuropathy (en, replaced) Iowa Type Amyloid Polyneuropathy (en, replaced) Finnish Type Familial Amyloid Neuropathy (en, replaced) Familial Amyloid Polyneuropathy, Type III (en, replaced) Amyloid Polyneuropathy, Iowa Type (en, replaced) |
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