| Descriptor English: | Amyloid Neuropathies | ||||||
| Descriptor Spanish: |
Neuropatías Amiloides
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| Descriptor Portuguese: | Neuropatias Amiloides | ||||||
| Descriptor French: | Neuropathies amyloïdes | ||||||
| Entry term(s): |
Amyloid Neuropathies, Secondary Amyloid Neuropathy Amyloid Neuropathy, Secondary Amyloid Polyneuropathies Amyloid Polyneuropathy Neuropathies, Amyloid Neuropathies, Secondary Amyloid Neuropathy, Amyloid Neuropathy, Secondary Amyloid Polyneuropathies, Amyloid Polyneuropathy, Amyloid Secondary Amyloid Neuropathies Secondary Amyloid Neuropathy |
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| Tree number(s): |
C10.668.829.050 C18.452.845.500.050 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017772 | ||||||
| Scope note: | Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) |
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| Annotation: | coord IM with specific neurol dis (IM) or specific nerve (IM); /genet: consider also AMYLOID NEUROPATHIES, FAMILIAL |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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: |
Amyloidosis (1967-1993) Peripheral Nervous System Diseases (1967-1993) |
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| Public MeSH Note: | 1994 |
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| History Note: | 1994 |
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| DeCS ID: | 31657 | ||||||
| Unique ID: | D017772 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1994/01/01 | ||||||
| Date of Entry: | 1993/06/30 | ||||||
| Revision Date: | 2009/07/06 |
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Amyloid Neuropathies
- Preferred
Amyloid Neuropathy, Secondary
- Narrower
| Concept UI |
M0026863 |
| Scope note | Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) |
| Preferred term | Amyloid Neuropathies |
| Entry term(s) |
Amyloid Neuropathy Amyloid Polyneuropathies Amyloid Polyneuropathy Neuropathies, Amyloid Neuropathy, Amyloid Polyneuropathies, Amyloid Polyneuropathy, Amyloid |
| Concept UI |
M0335819 |
| Preferred term | Amyloid Neuropathy, Secondary |
| Entry term(s) |
Amyloid Neuropathies, Secondary Neuropathies, Secondary Amyloid Neuropathy, Secondary Amyloid Secondary Amyloid Neuropathies Secondary Amyloid Neuropathy |
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