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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Muscular Atrophy, Spinal [Disease/Finding] | |
| Synonyms |
Spinal Amyotrophy Muscular Atrophy, Spinal Spinal Muscular Atrophy |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002063 |
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| altLabel |
Spinal Amyotrophy Muscular Atrophy, Spinal Spinal Muscular Atrophy
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| cui |
C0026847
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| May be treated by | ||
| MESH DEFINITION |
A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
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| MESH DUI |
D009134
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| MeSH name |
Muscular Atrophy, Spinal
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| MESH UI |
M0014250
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| NDFRT kind |
DISEASE_KIND
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| notation |
N0000002063
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| NUI |
N0000002063
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| prefLabel |
Muscular Atrophy, Spinal [Disease/Finding]
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| SNOMED CID |
5262007 192885003
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| tui |
T047
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| subClassOf |
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