Parkinson Disease 7, Autosomal Recessive Early-Onset

Preferred Label : Parkinson Disease 7, Autosomal Recessive Early-Onset;

NCIt synonyms : PARK7;

NCIt definition : An autosomal recessive subtype of Parkinson disease, caused by mutation(s) in the PARK7 gene, encoding Parkinson disease protein 7.;

Details

Origin ID

C198606;

Automatic exact mappings (from CISMeF team)
- Oncogene dj1 [OMIM gene]
Currated CISMeF NLP mapping
- Parkinson disease 7, autosomal recessive early-onset [OMIM Phenotype]
- Parkinson's disease 7 [DO Concept]
- parkinson disease 7, autosomal recessive Early-Onset [MeSH concept]
- parkinson disease 7, autosomal recessive Early-Onset [MeSH Supplementary Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
See also inter- (CISMeF)
- Parkinsonism associated deglycase [ORDO Gene]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- PARK7 Gene [NCIt concept]

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