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Amyloid Neuropathies
Hierarchy: | ∟ ∟ ∟ ∟ Amyloid Neuropathies 18 coordinate concepts1 subordinate concept∟ ∟ ∟ ∟ Amyloid Neuropathies 18 coordinate concepts1 subordinate conceptX |
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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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History note: | |
historyNote*: | 1994
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publicMeSHNote*: | 1994
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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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activeMeSHYear*: | |
dateCreated*: | 1993-06-30X |
dateEstablished*: | 1994-01-01X |
dateRevised*: | 2004-07-07X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | agsX |
recordOriginator*: | RAZX |
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Labels and equivalent concepts: | Amyloidineuropatiat (fi) XAmyloidineuropatia (fi, replaced) Amyloidihermosairaus (fi, replaced) Amyloidihermosairaudet (fi, replaced) Amyloidneuropatier (sv) Familjär amyloidos med polyneuropati (sv, replaced) Skelleftesjukan (sv, replaced) Neuropathies, Amyloid (en, replaced) Amyloid Polyneuropathies (en, replaced) |
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