Descriptor English: | Polyneuropathies | ||||||
Descriptor Spanish: |
Polineuropatías
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Descriptor Portuguese: | Polineuropatias | ||||||
Descriptor French: | Polyneuropathies | ||||||
Entry term(s): |
Acquired Polyneuropathies Acquired Polyneuropathy Critical Illness Polyneuropathies Critical Illness Polyneuropathy Familial Polyneuropathies Familial Polyneuropathy Inherited Polyneuropathies Inherited Polyneuropathy Motor Polyneuropathies Motor Polyneuropathy Polyneuropathies, Acquired Polyneuropathies, Critical Illness Polyneuropathies, Familial Polyneuropathies, Inherited Polyneuropathies, Motor Polyneuropathy Polyneuropathy, Acquired Polyneuropathy, Critical Illness Polyneuropathy, Familial Polyneuropathy, Inherited Polyneuropathy, Motor |
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Tree number(s): |
C10.668.829.800 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D011115 | ||||||
Scope note: | Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. |
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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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Public MeSH Note: | 2000; see POLYNEURITIS 1966-1999 |
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History Note: | 2000(1966) |
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DeCS ID: | 11553 | ||||||
Unique ID: | D011115 | ||||||
NLM Classification: | WL 520 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2000/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2013/07/09 |
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Polyneuropathies
- Preferred
Polyneuropathy, Motor
- Narrower
Polyneuropathy, Familial
- Narrower
Polyneuropathy, Acquired
- Narrower
Polyneuropathy, Critical Illness
- Narrower
Concept UI |
M0333806 |
Scope note | Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. |
Preferred term | Polyneuropathies |
Entry term(s) |
Polyneuropathy |
Concept UI |
M0336470 |
Preferred term | Polyneuropathy, Motor |
Entry term(s) |
Motor Polyneuropathies Motor Polyneuropathy Polyneuropathies, Motor |
Concept UI |
M0336469 |
Preferred term | Polyneuropathy, Familial |
Entry term(s) |
Familial Polyneuropathies Familial Polyneuropathy Inherited Polyneuropathies Inherited Polyneuropathy Polyneuropathies, Familial Polyneuropathies, Inherited Polyneuropathy, Inherited |
Concept UI |
M0336467 |
Preferred term | Polyneuropathy, Acquired |
Entry term(s) |
Acquired Polyneuropathies Acquired Polyneuropathy Polyneuropathies, Acquired |
Concept UI |
M0336468 |
Preferred term | Polyneuropathy, Critical Illness |
Entry term(s) |
Critical Illness Polyneuropathies Critical Illness Polyneuropathy Polyneuropathies, Critical Illness |
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