parkinson disease 7, autosomal recessive Early-Onset

Preferred Label : parkinson disease 7, autosomal recessive Early-Onset;

MeSH note : aka PARK7; associated with mutation of DJ1;

Origin ID

C565238;

UMLS CUI

C1853445;

Currated CISMeF NLP mapping
- Parkinson Disease 7, Autosomal Recessive Early-Onset [NCIt concept]
- Parkinson disease 7, autosomal recessive early-onset [OMIM Phenotype]
- Parkinson's disease 7 [DO Concept]
MeSH term(s) associated for indexing
- parkinson disease [MeSH Descriptor]
Record concept(s)
- parkinson disease 7, autosomal recessive Early-Onset [MeSH concept]
See also inter- (CISMeF)
- Parkinsonism associated deglycase [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Parkinson Disease 7, Autosomal Recessive Early-Onset [NCIt concept]
- Parkinson disease 7, autosomal recessive early-onset [OMIM Phenotype]
- Parkinson's disease 7 [DO Concept]
- Parkinsonism associated deglycase [ORDO Gene]