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Motor Neuron Disease
Hierarchy: | ∟ ∟ ∟ Motor Neuron Disease 19 coordinate concepts4 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Motor Neuron Disease 19 coordinate concepts4 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Annotation: | GEN or unspecified; prefer specifics
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historyNote*: | 92
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publicMeSHNote*: | 92
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Scope note: | Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)
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activeMeSHYear*: | |
dateCreated*: | 1991-06-21X |
dateEstablished*: | 1992-01-01X |
dateRevised*: | 2004-07-28X |
recordAuthorizer*: | jlsX |
recordMaintainer*: | jlsX |
recordOriginator*: | AGSX |
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Labels and equivalent concepts: | Motoneuronisairaus (fi) XMotoneuronisairaudet (fi, replaced) Motoneuronitaudit (fi, replaced) Motoneuronitauti (fi, replaced) Motorneuronsjukdom (sv) Upper Motor Neuron Disease (en, replaced) Secondary Motor Neuron Disease (en, replaced) Motor Neuron Disease, Familial (en, replaced) Motor System Disease (en, replaced) Primary Lateral Sclerosis (en, replaced) Lower Motor Neuron Disease (en, replaced) Morbus motoneuronalis (la-FI, replaced) |
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