parkinson disease, familial, type 1

Preferred Label : parkinson disease, familial, type 1;

MeSH note : aka PARK1;

CISMeF synonym : atypical parkinson disease;

MeSH synonym : parkinson disease, autosomal dominant; lewy body parkinsonism;

Details

Origin ID

C566823;

UMLS CUI

C3489791;

Automatic exact mappings (from CISMeF team)
- Parkinson disease synuclein gene mutation 4q21.23 [ICD-11 More detail]
CISMeF manual mappings
- Parkinson's disease 1 [DO Concept]
Currated CISMeF NLP mapping
- Parkinson disease 1, autosomal dominant [OMIM Phenotype]
- autosomal dominant Parkinson disease [Disease (Nov.)]
MeSH term(s) associated for indexing
- parkinson disease [MeSH Descriptor]
Record concept(s)
- atypical parkinson disease [MeSH concept]
- parkinson disease, familial, type 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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