Details of Disease | DrugMAP

General Information of Disease (ID: DIS1S1E4)

Disease Name	Parkinson disease 11, autosomal dominant, susceptibility to
Synonyms	PARK11; susceptibility to autosomal dominant Parkinson disease 11; hereditary late onset Parkinson disease caused by mutation in GIGYF2; GIGYF2 hereditary late onset Parkinson disease; Parkinson disease 11; Parkinson disease 11, autosomal dominant, susceptibility to
Definition	An inherited susceptibility or predisposition to developing late onset Parkinson disease, in which the cause of the disease is a mutation in the GIGYF2 gene.
Disease Hierarchy	DIS98MYE: Inherited disease susceptibility DIS1S1E4: Parkinson disease 11, autosomal dominant, susceptibility to
Disease Identifiers	MONDO ID MONDO_0011896 UMLS CUI C4083045 OMIM ID 607688 MedGen ID 896658

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
GIGYF2	OTFNVEJ4	Moderate	Autosomal dominant	[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.