Parkinson disease LRRK2 gene mutation 12p11.23-q13.11

Preferred Label : Parkinson disease LRRK2 gene mutation 12p11.23-q13.11;

ICD-11 definition : LRRK2 mutation is responsible for approximately 2 percent of the apparently sporadic PD in the western world and up to 30% in certain populations.;

ICD-11 synonym : PARK8;

Details

Origin ID

920819080;

Automatic exact mappings (from CISMeF team)
- Parkinson Disease 8, Autosomal Dominant [NCIt concept]
- Parkinson disease 8, autosomal dominant [OMIM Phenotype]
See also inter- (CISMeF)
- LRRK2 wt Allele [NCIt concept]
- leucine rich repeat kinase 2 [ORDO Gene]

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