Alpha-synuclein signaling

No Pathway Network information available for Alpha-synuclein signaling

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

Disorders associated with Alpha-synuclein signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Early-onset parkinson's diseaseEnrichmentPARK7, PRKN, SNCA, UCHL18.28
2Parkinson disease, late-onsetEnrichmentPRKN, SNCA3.02
3Parkinson disease 1, autosomal dominantEnrichmentSNCA2.72
4Dystonia 1, torsion, autosomal dominantEnrichmentTOR1A2.72
5Cardiac valvular dysplasia 1EnrichmentPLD12.72
6Parkinson disease 4, autosomal dominantEnrichmentSNCA2.72
7Leprosy 2EnrichmentPRKN2.72
8Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.72
9Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.72
10Parkinsonism-dystonia 1, infantile-onsetEnrichmentSLC6A32.72
11Parkinson disease 7, autosomal recessive early-onsetEnrichmentPARK72.72
12Parkinson disease 5, autosomal dominantEnrichmentUCHL12.72
13Immunodeficiency 22EnrichmentLCK2.72
14Okur-chung neurodevelopmental syndromeEnrichmentCSNK2A12.72
15Arthrogryposis multiplex congenita 5EnrichmentTOR1A2.72
16Classic dopamine transporter deficiency syndromeEnrichmentSLC6A32.72
17ColitisEnrichmentSYK2.72
18Dyt1 early-onset isolated dystoniaEnrichmentTOR1A2.72
19Parkinsonism-dystonia, infantileEnrichmentSLC6A32.72
20DystoniaEnrichmentTH, TOR1A2.69
21Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1EnrichmentPARK72.42
22Parkinson disease 12EnrichmentPRKN2.42
23Seizures, benign familial infantile, 2EnrichmentPRRT22.42
24Segawa syndrome, autosomal recessiveEnrichmentTH2.42
25Spastic paraplegia 76, autosomal recessiveEnrichmentCAPN12.42
26Houge-janssens syndrome 1EnrichmentPPP2R5D2.42
27Spastic paraplegia 79b, autosomal recessiveEnrichmentUCHL12.42
28Spinocerebellar ataxia 48EnrichmentSTUB12.42
29Parkinson disease 15, autosomal recessive early-onsetEnrichmentSNCA2.42
30Hereditary spastic paraplegia 79aEnrichmentUCHL12.42
31Spastic paraplegia 79a, autosomal dominant, with ataxiaEnrichmentUCHL12.42
32ArthritisEnrichmentSYK2.42
33Prrt2-related disorderEnrichmentPRRT22.42
34Dystonia, dopa-responsiveEnrichmentTH2.24
35Glut1 deficiency syndrome 2EnrichmentPRRT22.24
36Torsion dystonia 1EnrichmentTOR1A2.24
37Paroxysmal nonkinesigenic dyskinesia 1EnrichmentPRRT22.12
38Episodic kinesigenic dyskinesia 1EnrichmentPRRT22.12
39Tobacco addictionEnrichmentSLC6A32.12
40Familial paroxysmal nonkinesigenic dyskinesiaEnrichmentPRRT22.12
41Familial or sporadic hemiplegic migraineEnrichmentPRRT22.12
42Complex hereditary spastic paraplegiaEnrichmentPRKN2.12
43Dementia, lewy bodyEnrichmentSNCA2.02
44Parkinson disease 2, autosomal recessive juvenileEnrichmentPRKN2.02
45Convulsions, familial infantile, with paroxysmal choreoathetosisEnrichmentPRRT22.02
46Parkin type of early-onset parkinson diseaseEnrichmentPRKN2.02
47Self-limited infantile epilepsyEnrichmentPRRT22.02
48Dystonia 11, myoclonicEnrichmentTOR1A1.94
49Parkinson disease 6, autosomal recessive early-onsetEnrichmentPARK71.94
50Spinocerebellar ataxia, autosomal recessive 16EnrichmentSTUB11.94
51Autism spectrum disorderEnrichmentCSNK2A1, PRKN1.74
52Immune deficiency diseaseEnrichmentSYK1.68
53Lung cancer susceptibility 3EnrichmentPRKN1.58
54Generalized epilepsy with febrile seizures plusEnrichmentPRRT21.58
55Parkinson's diseaseEnrichmentPRKN1.45
56Lung cancerEnrichmentPRKN1.22
57Severe combined immunodeficiencyEnrichmentLCK1.21
58Systemic lupus erythematosusEnrichmentUBE2L31.14
59SchizophreniaEnrichmentPRKN0.97
60AutismEnrichmentPRKN0.89
61Ovarian cancerEnrichmentPRKN0.75
62Complex neurodevelopmental disorderEnrichmentCSNK2A10.67

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