parkinson disease 3, autosomal dominant lewy body

Preferred Label : parkinson disease 3, autosomal dominant lewy body;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566852;

UMLS CUI

C1865581;

Currated CISMeF NLP mapping
- Parkinson disease 3, autosomal dominant [OMIM Phenotype]
Related record
- parkinson disease 3, autosomal dominant lewy body [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Parkinson disease 3, autosomal dominant [OMIM Phenotype]