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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000002063
http://purl.bioontology.org/ontology/NDFRT/N0000002063
|
|---|---|
| Preferred Name | Muscular Atrophy, Spinal [Disease/Finding] |
| Synonyms |
Spinal Amyotrophy
Muscular Atrophy, Spinal
Spinal Muscular Atrophy
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Spinal Amyotrophy
Muscular Atrophy, Spinal
Spinal Muscular Atrophy
|
|---|---|
| prefLabel | Muscular Atrophy, Spinal [Disease/Finding]
|
| 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)
|
| MESH DUI | D009134
|
| MESH UI | M0014250
|
| MeSH name | Muscular Atrophy, Spinal
|
| type | |
| tui | T047
|
| SNOMED CID |
5262007
192885003
|
| May be treated by | |
| notation | N0000002063
|
| Semantic type UMLS property | |
| NUI | N0000002063
|
| cui | C0026847
|
| NDFRT kind | DISEASE_KIND
|
| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |