Parkinson disease 3, autosomal dominant

Preferred Label : Parkinson disease 3, autosomal dominant;

Symbol : PARK3;

CISMeF acronym : PARK3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Parkinson disease 3, autosomal dominant lewy body;

Description : For a phenotypic description and a discussion of genetic heterogeneity of Parkinson disease, see 168600.;

Prefixed ID : %602404;

Details

Origin ID

602404;

UMLS CUI

C1865581;

Automatic exact mappings (from CISMeF team)
- Parkinson disease 3 (autosomal dominant, Lewy body) [HGNC gene]
- Parkinson's disease 3 [DO Concept]
Broader ORDO disease(s)
- Young-onset Parkinson disease [ORDO Disease]
CISMeF manual mappings
- parkinson disease 3 [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- parkinson disease 3, autosomal dominant lewy body [MeSH concept]
- parkinson disease 3, autosomal dominant lewy body [MeSH Supplementary Concept]
DO Cross reference
- Parkinson's disease 3 [DO Concept]
ORDO concept(s)
- Young-onset Parkinson disease [ORDO Disease]
See also inter- (CISMeF)
- Young-onset Parkinson disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- parkinson disease 3, autosomal dominant lewy body [MeSH Supplementary Concept]
- parkinson disease 3, autosomal dominant lewy body [MeSH concept]

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