parkinsonian disorders

Preferred Label : parkinsonian disorders;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0328250;

UMLS CUI

C0242422;

Automatic exact mappings (from CISMeF team)
- parkinsonism [TUV Term]
- parkinsonism [TUV Concept]
Currated CISMeF NLP mapping
- PARKINSONISM [WHO-ART Included Term]
- Parkinson's disease [ICD-9 code]
- Parkinsonism [HPO term]
- Parkinsonism [MedDRA Preferred Term]
- Parkinsonism [ICD-11 Category]
- Parkinsonism (disorder) [SNOMED CT concept]
- parkinsonism [ICPC-2 Rubric]
- parkinsonism, nos [SNOMED Notion]
MeSH narrower concept(s)
- autosomal dominant juvenile parkinson disease [MeSH concept]
- autosomal dominant parkinsonism [MeSH concept]
- autosomal recessive juvenile parkinson disease [MeSH concept]
- autosomal recessive parkinsonism [MeSH concept]
- familial juvenile parkinsonism [MeSH concept]
- parkinsonism, experimental [MeSH concept]
- parkinsonism, juvenile [MeSH concept]
Related MeSH concept(s)
- ramsay hunt paralysis syndrome [MeSH concept]
Related record
- parkinsonian disorders [MeSH Descriptor]
See also inter- (CISMeF)
- Parkinsonism [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypokinetic-rigid syndrome [MedDRA LLT]
- PARKINSONISM [WHO-ART Included Term]
- Parkinsonism [MedDRA Preferred Term]
- Parkinsonism [HPO term]
- Parkinsonism [PASCAL descriptor]
- Parkinsonism [NCIt concept]
- Parkinsonism (disorder) [SNOMED CT concept]
- Rare parkinsonian disorder [ORDO Disease]
- parkinsonism [ICPC-2 Rubric]
- parkinsonism [Disease (Nov.)]
- parkinsonism, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

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