Parkinson's disease pathway

No Pathway Network information available for Parkinson's disease pathway

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Parkinson's disease pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Early-onset parkinson's diseaseEnrichmentHTRA2, LRRK2, PARK7, PINK1, PRKN, SNCA, UCHL110.88
2Parkinson disease, late-onsetEnrichmentATXN2, LRRK2, PRKN, SNCA6.27
3Parkinson's diseaseEnrichmentATXN2, LRRK2, PRKN4.72
4Parkinson disease 6, autosomal recessive early-onsetEnrichmentPARK7, PINK13.94
5Parkinson disease 1, autosomal dominantEnrichmentSNCA2.55
6Parkinson disease 13, autosomal dominantEnrichmentHTRA22.55
7Parkinson disease 4, autosomal dominantEnrichmentSNCA2.55
8Leprosy 2EnrichmentPRKN2.55
9Thrombocytopenia 4EnrichmentCYCS2.55
10Parkinsonism-dystonia 1, infantile-onsetEnrichmentSLC6A32.55
11Parkinson disease 7, autosomal recessive early-onsetEnrichmentPARK72.55
12Parkinson disease 5, autosomal dominantEnrichmentUCHL12.55
13Leukodystrophy, hypomyelinating, 15EnrichmentEPRS12.55
14Classic dopamine transporter deficiency syndromeEnrichmentSLC6A32.55
15Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.55
16Amyotrophic lateral sclerosis type 13EnrichmentATXN22.55
17Parkinsonism-dystonia, infantileEnrichmentSLC6A32.55
18Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1EnrichmentPARK72.25
19Parkinson disease 12EnrichmentPRKN2.25
20Vexas syndromeEnrichmentUBA12.25
21Parkinson disease 8, autosomal dominantEnrichmentLRRK22.25
22Segawa syndrome, autosomal recessiveEnrichmentTH2.25
23Aromatic l-amino acid decarboxylase deficiencyEnrichmentDDC2.25
24Spinocerebellar ataxia 2EnrichmentATXN22.25
25Spastic paraplegia 79b, autosomal recessiveEnrichmentUCHL12.25
26Spinal muscular atrophy, x-linked 2EnrichmentUBA12.25
27Parkinson disease 15, autosomal recessive early-onsetEnrichmentSNCA2.25
28Hereditary spastic paraplegia 79aEnrichmentUCHL12.25
29Spastic paraplegia 79a, autosomal dominant, with ataxiaEnrichmentUCHL12.25
30Submucosal cleft palateEnrichmentUBB2.25
31Cleft hard palateEnrichmentUBB2.25
32Dystonia, dopa-responsiveEnrichmentTH2.08
33Klippel-feil syndrome 1, autosomal dominantEnrichmentLRRK22.08
34Uvula, bifidEnrichmentUBB2.08
35Cleft soft palateEnrichmentUBB2.08
36Tobacco addictionEnrichmentSLC6A31.95
373-methylglutaconic aciduria, type viiiEnrichmentHTRA21.95
38Complex hereditary spastic paraplegiaEnrichmentPRKN1.95
39Dementia, lewy bodyEnrichmentSNCA1.86
40Parkinson disease 2, autosomal recessive juvenileEnrichmentPRKN1.86
41Parkin type of early-onset parkinson diseaseEnrichmentPRKN1.86
42Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.86
43Machado-joseph diseaseEnrichmentLRRK21.78
44Autosomal dominant cerebellar ataxiaEnrichmentLRRK21.60
45Lung cancer susceptibility 3EnrichmentPRKN1.41
46RasopathyEnrichmentDDC1.15
47Lung cancerEnrichmentPRKN1.07
48DystoniaEnrichmentTH1.03
49Systemic lupus erythematosusEnrichmentUBE2L30.98
50ThrombocytopeniaEnrichmentCYCS0.90
51Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentATXN20.82
52SchizophreniaEnrichmentPRKN0.82
53AutismEnrichmentPRKN0.74
54Ovarian cancerEnrichmentPRKN0.61
55Autism spectrum disorderEnrichmentPRKN0.58

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