parkinson disease 13

Preferred Label : parkinson disease 13;

MeSH synonym : PARK13;

Origin ID

C565204;

UMLS CUI

C3496588;

Automatic exact mappings (from CISMeF team)
- HtrA serine peptidase 2 [ORDO Gene]
Currated CISMeF NLP mapping
- Parkinson disease 13, autosomal dominant, susceptibility to [OMIM Phenotype]
MeSH term(s) associated for indexing
- parkinson disease [MeSH Descriptor]
Record concept(s)
- parkinson disease 13 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]