| Descriptor English: | Amyloid Neuropathies, Familial | ||||||
| Descriptor Spanish: |
Neuropatías Amiloides Familiares
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| Descriptor Portuguese: | Neuropatias Amiloides Familiares | ||||||
| Descriptor French: | Neuropathies amyloïdes familiales | ||||||
| Entry term(s): |
Amyloid Neuropathy Type 1 Amyloid Neuropathy, Familial Amyloid Polyneuropathies, Familial Amyloid Polyneuropathy, British Type Amyloid Polyneuropathy, Familial Amyloid Polyneuropathy, Iowa Type Amyloid Polyneuropathy, Swiss Type Amyloid Syndrome, Neuropathic Amyloid Syndromes, Neuropathic Amyloidoses, Hereditary Neuropathic Amyloidoses, Portuguese Polyneuritic Amyloidosis, Hereditary Neuropathic Amyloidosis, Portuguese Polyneuritic Appalachian Type Familial Amyloid Polyneuropathy British Type Amyloid Polyneuropathy Cerebral Amyloid Angiopathy, British Type Familial Amyloid Neuropathies Familial Amyloid Neuropathy Familial Amyloid Neuropathy, Andrade Type Familial Amyloid Neuropathy, Finnish Type Familial Amyloid Neuropathy, Portuguese Type Familial Amyloid Polyneuropathies Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Appalachian Type Familial Amyloid Polyneuropathy, Jewish Type Familial Amyloid Polyneuropathy, Type I Familial Amyloid Polyneuropathy, Type II Familial Amyloid Polyneuropathy, Type III Familial Amyloid Polyneuropathy, Type IV Familial Amyloid Polyneuropathy, Type V Familial Amyloid Polyneuropathy, Type VI Familial Portuguese Polyneuritic Amyloidosis Finnish Type Familial Amyloid Neuropathy Hereditary Neuropathic Amyloidoses Hereditary Neuropathic Amyloidosis Iowa Type Amyloid Polyneuropathy Jewish Type Familial Amyloid Polyneuropathy Neuropathic Amyloid Syndrome Neuropathic Amyloid Syndromes Neuropathic Amyloidoses, Hereditary Neuropathic Amyloidosis, Hereditary Neuropathies, Familial Amyloid Neuropathy, Familial Amyloid Polyneuritic Amyloidoses, Portuguese Polyneuritic Amyloidosis, Portuguese Polyneuropathies, Familial Amyloid Polyneuropathy, Familial Amyloid Portuguese Polyneuritic Amyloidoses Portuguese Polyneuritic Amyloidosis Portuguese Type Familial Amyloid Neuropathy Swiss Type Amyloid Polyneuropathy Type I Familial Amyloid Polyneuropathy Type II Familial Amyloid Polyneuropathy Type III Familial Amyloid Polyneuropathy Type IV Familial Amyloid Polyneuropathy Type V Familial Amyloid Polyneuropathy Type VI Familial Amyloid Polyneuropathy Wohlwill Andrade Syndrome Wohlwill Corino Andrade Syndrome Wohlwill-Andrade Syndrome Wohlwill-Corino Andrade Syndrome |
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| Tree number(s): |
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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D028227 | ||||||
| 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Amyloid Neuropathies (1994-2001) Amyloidosis (1967-1993) Peripheral Nervous System Diseases (1967-1993) |
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| Public MeSH Note: | 2002; see AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES see AMYLOID NEUROPATHIES 1994-2001 |
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| History Note: | 2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001 |
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| DeCS ID: | 36014 | ||||||
| Unique ID: | D028227 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2002/01/01 | ||||||
| Date of Entry: | 2001/07/25 | ||||||
| Revision Date: | 2018/02/28 |
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Amyloid Neuropathies, Familial
- Preferred
Familial Amyloid Polyneuropathy, Type VI
- Narrower
Amyloid Polyneuropathy, British Type
- Narrower
Amyloid Polyneuropathy, Iowa Type
- Narrower
Familial Amyloid Neuropathy, Portuguese Type
- Narrower
Familial Amyloid Polyneuropathy, Appalachian Type
- Narrower
Familial Amyloid Polyneuropathy, Jewish Type
- Narrower
Familial Amyloid Polyneuropathy, Type IV
- Narrower
Familial Amyloid Polyneuropathy, Type V
- Narrower
Amyloid Polyneuropathy, Swiss Type
- Narrower
| Concept UI |
M0026861 |
| 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. |
| Preferred term | Amyloid Neuropathies, Familial |
| Entry term(s) |
Amyloid Neuropathy, Familial Amyloid Polyneuropathies, Familial Amyloid Polyneuropathy, Familial Amyloidoses, Hereditary Neuropathic Amyloidosis, Hereditary Neuropathic Familial Amyloid Neuropathies Familial Amyloid Neuropathy Familial Amyloid Polyneuropathies Familial Amyloid Polyneuropathy Hereditary Neuropathic Amyloidoses Hereditary Neuropathic Amyloidosis Neuropathic Amyloidoses, Hereditary Neuropathic Amyloidosis, Hereditary Neuropathies, Familial Amyloid Neuropathy, Familial Amyloid Polyneuropathies, Familial Amyloid Polyneuropathy, Familial Amyloid |
| Concept UI |
M0393103 |
| Preferred term | Familial Amyloid Polyneuropathy, Type VI |
| Entry term(s) |
Type VI Familial Amyloid Polyneuropathy |
| Concept UI |
M0335820 |
| Preferred term | Amyloid Polyneuropathy, British Type |
| Entry term(s) |
British Type Amyloid Polyneuropathy Cerebral Amyloid Angiopathy, British Type |
| Concept UI |
M000640324 |
| Preferred term | Amyloid Polyneuropathy, Iowa Type |
| Entry term(s) |
Familial Amyloid Polyneuropathy, Type III Iowa Type Amyloid Polyneuropathy Type III Familial Amyloid Polyneuropathy |
| Concept UI |
M0335929 |
| Preferred term | Familial Amyloid Neuropathy, Portuguese Type |
| Entry term(s) |
Amyloid Neuropathy Type 1 Amyloid Syndrome, Neuropathic Amyloid Syndromes, Neuropathic Amyloidoses, Portuguese Polyneuritic Amyloidosis, Portuguese Polyneuritic Familial Amyloid Neuropathy, Andrade Type Familial Amyloid Polyneuropathy, Type I Familial Portuguese Polyneuritic Amyloidosis Neuropathic Amyloid Syndrome Neuropathic Amyloid Syndromes Polyneuritic Amyloidoses, Portuguese Polyneuritic Amyloidosis, Portuguese Portuguese Polyneuritic Amyloidoses Portuguese Polyneuritic Amyloidosis Portuguese Type Familial Amyloid Neuropathy Type I Familial Amyloid Polyneuropathy Wohlwill Andrade Syndrome Wohlwill Corino Andrade Syndrome Wohlwill-Andrade Syndrome Wohlwill-Corino Andrade Syndrome |
| Concept UI |
M0335919 |
| Preferred term | Familial Amyloid Polyneuropathy, Appalachian Type |
| Entry term(s) |
Appalachian Type Familial Amyloid Polyneuropathy |
| Concept UI |
M0335928 |
| Preferred term | Familial Amyloid Polyneuropathy, Jewish Type |
| Entry term(s) |
Jewish Type Familial Amyloid Polyneuropathy |
| Concept UI |
M0335930 |
| Preferred term | Familial Amyloid Polyneuropathy, Type IV |
| Entry term(s) |
Type IV Familial Amyloid Polyneuropathy |
| Concept UI |
M0335920 |
| Preferred term | Familial Amyloid Polyneuropathy, Type V |
| Entry term(s) |
Familial Amyloid Neuropathy, Finnish Type Finnish Type Familial Amyloid Neuropathy Type V Familial Amyloid Polyneuropathy |
| Concept UI |
M0335918 |
| Preferred term | Amyloid Polyneuropathy, Swiss Type |
| Entry term(s) |
Familial Amyloid Polyneuropathy, Type II Swiss Type Amyloid Polyneuropathy Type II Familial Amyloid Polyneuropathy |
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