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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 08-11-2017 |
Symbol | PARK21 |
Location | 3q22.1 |
Name | Parkinson disease 21 |
Corresponding gene | DNAJC13 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Related entries | including also cases of essential tremor (PMID: 25118025) |
Function/system disorder | neurology |
Type | disease |
Remark(s) |