muscular atrophy, spinal

Preferred Label : muscular atrophy, spinal;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0014250;

UMLS CUI

C0026847;

Automatic exact mappings (from CISMeF team)
- Progressive muscular atrophy [MedDRA Preferred Term]
- Spinal muscular atrophy [LOINC component]
- Spinal muscular atrophy, unspecified [ICD-10 Sub-category (who)]
- progressive muscular atrophy [SNOMED Notion]
MeSH narrower concept(s)
- bulbospinal neuronopathy [MeSH concept]
- distal spinal muscular atrophy [MeSH concept]
- hereditary motor neuronopathy [MeSH concept]
- myelopathic muscular atrophy [MeSH concept]
- oculopharyngeal spinal muscular atrophy [MeSH concept]
- progressive muscular atrophy [MeSH concept]
- progressive proximal myelopathic muscular atrophy [MeSH concept]
- scapuloperoneal form of spinal muscular atrophy [MeSH concept]
Related record
- muscular atrophy, spinal [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinal Muscular Atrophy [NCIt concept]
- Spinal amyotrophy [MedDRA LLT]
- Spinal muscular atrophy [ICD-9 code]
- Spinal muscular atrophy [MedDRA Preferred Term]
- Spinal muscular atrophy [HPO term]
- Spinal muscular atrophy [ICD-11 Category]
- Spinal muscular atrophy [LOINC component]
- Spinal muscular atrophy (disorder) [SNOMED CT concept]
- Spinal muscular atrophy, unspecified [MedDRA LLT]
- Spinal muscular atrophy, unspecified [ICD-10 Sub-category]
- Spinal muscular atrophy, unspecified [ICD-9 code]
- spinal muscular atrophy [MedlinePlus Topic]
- spinal muscular atrophy [DO Concept]
- spinal muscular atrophy [Disease (Nov.)]
- spinal muscular atrophy, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

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