Progressive Muscular Atrophy

Preferred Label : Progressive Muscular Atrophy;

NCIt definition : A rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation.;

Details

Origin ID

C85027;

UMLS CUI

C0917981;

Automatic exact mappings (from CISMeF team)
- Motor neuron disease [ICD-10 Sub-category]
- Motor neuron disease [ICD-10 Sub-category (who)]
- Progressive muscular atrophy [ORDO Disease]
- Progressive muscular atrophy [ICD-11 Subcategory]
- Progressive muscular atrophy [ICD-9 code]
- muscular atrophy, spinal [MeSH Descriptor]
Currated CISMeF NLP mapping
- Progressive muscular atrophy [MedDRA Preferred Term]
- Progressive muscular atrophy (disorder) [SNOMED CT concept]
- Progressive spinal muscular atrophy [HPO term]
- progressive muscular atrophy [DO Concept]
- progressive muscular atrophy [Disease (Nov.)]
- progressive muscular atrophy [MeSH concept]
- progressive muscular atrophy [SNOMED Notion]
DO Cross reference
- progressive muscular atrophy [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Progressive muscular atrophy [ORDO Disease]
- Progressive muscular atrophy [ICD-9 code]
- Progressive muscular atrophy [MedDRA Preferred Term]
- Progressive muscular atrophy (disorder) [SNOMED CT concept]
- progressive muscular atrophy [DO Concept]
- progressive muscular atrophy [Disease (Nov.)]
- progressive muscular atrophy [SNOMED Notion]
- progressive muscular atrophy [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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