Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.600 Biomarker GENOMICS_ENGLAND Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78). 28137957

2017
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.600 Biomarker GENOMICS_ENGLAND Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. 21060012

2010