Parkinson disease

Disease Term Disease ID Gene Symbol Classification References Source
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder) C1854182 SNCA Causal Pathogenic evidence from ClinVar - ClinVar
Parkinsonian Disorders C0242422 SNCA Causal Pathogenic evidence from ClinVar 20464527, 22319455, 23046578, 23295396, 26075822, 26558463, 26687234, 27026137, 27324791 ClinVar
SYNJ1 Causal Pathogenic evidence from ClinVar - ClinVar
VPS13C Causal Pathogenic evidence from ClinVar - ClinVar
VPS35 Causal Pathogenic evidence from ClinVar - ClinVar
A2M Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ABCA7 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ADH1C Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
AFG3L2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ALDH1A1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25045800 -
ALDH1A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25045800 -
AP5Z1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
APOE Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
APP Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ATP13A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23046578 -
ATP1A3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 15260953 -
ATP6AP2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ATXN2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Young-onset Parkinson disease 2828 SNCA Causal Pathogenic evidence from ClinVar - ClinVar
SYNJ1 Causal Pathogenic evidence from ClinVar - ClinVar
VPS13C Causal Pathogenic evidence from ClinVar - ClinVar
PARKINSON DISEASE 20, EARLY-ONSET C3809824 SYNJ1 Causal Pathogenic evidence from ClinVar 23804563, 23804577, 25316601, 27435091, 27496670, 27869329 ClinVar
Parkinson Disease C0030567 VPS13C Causal Pathogenic evidence from ClinVar 26942284 ClinVar
VPS35 Causal Pathogenic evidence from ClinVar 25149416 ClinVar
ABCB1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 20558393 -
ADAMTSL1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 17052657 -
ADARB2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25475535 -
AGAP1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 28892059 -
AIF1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 19276553 -
APOE Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 30957308 -
ATP13A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 21060012, 23628791, 25149416, 28137957 -
PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET C4225186 VPS13C Causal Pathogenic evidence from ClinVar 26942284, 28862745 ClinVar
PARKINSON DISEASE 17 C3280133 VPS35 Causal Pathogenic evidence from ClinVar 21763482, 21763483, 22517097, 23395371, 23408866, 24819384, 24854799, 24980502 ClinVar
Parkinson Disease, Secondary Vascular C0751414 ABCB1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 26457621 -
ATP13A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22285144 -
Secondary Parkinson Disease C0030569 ABCB1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 26457621 -
ATP13A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22285144 -
PARKINSON DISEASE, MITOCHONDRIAL (disorder) C1838867 ADH1B Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ADH1C Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
PARKINSON DISEASE, LATE-ONSET C3160718 ADH1C Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ATXN2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
ATXN3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Autosomal Dominant Juvenile Parkinson Disease C0752097 ALDH1A1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25045800 -
ALDH1A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25045800 -
ATP13A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23046578 -
ATP1A3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 15260953 -
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE C1868675 ALDH1A1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25045800 -
ALDH1A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25045800 -
ATP13A2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23046578 -
ATP1A3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 15260953 -