Striatonigral Degeneration

Preferred Label : Striatonigral Degeneration;

NCIt definition : A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements.;

Codes from synonyms : G23.2;

Details

Origin ID

C125695;

UMLS CUI

C0270733;

Automatic exact mappings (from CISMeF team)
- Multiple system atrophy, parkinsonian type [ORDO Disease]
- Striatonigral degeneration [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Striatonigral degeneration [ICD-10 Sub-category]
- Striatonigral degeneration [ICD-10 Sub-category (who)]
- Striatonigral degeneration (disorder) [SNOMED CT concept]
- striatonigral degeneration [MeSH concept]
- striatonigral degeneration [MeSH Descriptor]
- striatonigral degeneration [SNOMED Notion]
- striatonigral degeneration [DO Concept]
- striatonigral degeneration [Disease (Nov.)]
DO Cross reference
- striatonigral degeneration [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)
- Striatonigral degeneration [ICD-10 Sub-category]
- Striatonigral degeneration (disorder) [SNOMED CT concept]
- striatonigral degeneration [SNOMED Notion]
- striatonigral degeneration [DO Concept]
- striatonigral degeneration [MeSH Descriptor]
- striatonigral degeneration [MeSH concept]
- striatonigral degeneration [Disease (Nov.)]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- mCode Elixhauser Neurological Movement Disorder Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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