Parkinson disease UCHL-1 gene mutations 4p14 - CISMeF

" /> Parkinson disease UCHL-1 gene mutations 4p14 - CISMeF

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Parkinson disease UCHL-1 gene mutations 4p14ICD-11 More detail

Preferred Label : Parkinson disease UCHL-1 gene mutations 4p14;

ICD-11 synonym : PARK5;

Details

Origin ID

1067231592;

Automatic exact mappings (from CISMeF team)
- Parkinson disease 5, autosomal dominant, susceptibility to [OMIM Phenotype]
- UCHL1 wt Allele [NCIt concept]
- ubiquitin C-terminal hydrolase L1 [ORDO Gene]

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08/05/2025

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