Details of Disease

General Information of Disease (ID: DISKIOCW)

Disease Name Juvenile onset Parkinson disease 19A
Synonyms
Parkinson disease 19A, juvenile-onset; Parkinson disease 19, juvenile-onset; Parkinson disease 19B, early-onset; juvenile onset Parkinson's disease 19A; Park19, formerly; PARK19A; PARK19; Parkinson disease caused by mutation in DNAJC6; juvenile onset Parkinson disease type 19A; juvenile onset Parkinson disease 19A; DNAJC6 Parkinson disease
Definition Any Parkinson disease in which the cause of the disease is a mutation in the DNAJC6 gene.
Disease Hierarchy
DISYXFE3: Atypical juvenile parkinsonism
DISNT5BI: Juvenile-onset Parkinson disease
DISQVHKL: Parkinson disease
DISKIOCW: Juvenile onset Parkinson disease 19A
Disease Identifiers
MONDO ID
MONDO_0014231
UMLS CUI
C3809811
OMIM ID
615528
MedGen ID
816141

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
DNAJC6 OT1P6ZIE Strong Autosomal recessive [1]
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References

1 The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.