Effects of Botulinum toxin

No Pathway Network information available for Effects of Botulinum toxin

Pathways in the Effects of Botulinum toxin SuperPath

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

Disorders associated with Effects of Botulinum toxin SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1AutismEnrichmentCHRNA1, STX1A, STXBP14.93
2Developmental and epileptic encephalopathyEnrichmentSNAP25, STXBP13.61
3Warburg micro syndrome 2EnrichmentRAB3GAP23.18
4Developmental and epileptic encephalopathy 117EnrichmentSNAP253.18
5Baker-gordon syndromeEnrichmentSYT13.18
6Cone-rod dystrophy 7EnrichmentRIMS13.18
7Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movementsEnrichmentVAMP23.18
8Epilepsy with generalized tonic-clonic seizuresEnrichmentSNAP253.18
9Autosomal recessive spastic paraplegia type 69EnrichmentRAB3GAP23.18
109q33.3q34.11 microdeletion syndromeEnrichmentSTXBP12.88
11Gyrate atrophy of choroid and retinaEnrichmentRIMS12.70
12Autism spectrum disorderEnrichmentRIMS1, STXBP12.65
13Warburg micro syndrome 1EnrichmentRAB3GAP22.58
14Developmental and epileptic encephalopathy 2EnrichmentSNAP252.58
15Developmental and epileptic encephalopathy 4EnrichmentSTXBP12.58
16Myasthenic syndrome, congenital, 1b, fast-channelEnrichmentCHRNA12.58
17MicrocephalyEnrichmentSNAP25, STXBP12.55
18Martsolf syndrome 1EnrichmentRAB3GAP22.48
19Myasthenic syndrome, congenital, 1a, slow-channelEnrichmentCHRNA12.33
20Focal epilepsyEnrichmentSNAP252.33
21Multiple pterygium syndrome, lethal typeEnrichmentCHRNA12.28
22Presynaptic congenital myasthenic syndromesEnrichmentSNAP252.14
23Postsynaptic congenital myasthenic syndromesEnrichmentCHRNA12.10
24Stereotypic movement disorderEnrichmentSNAP252.07
25Congenital myasthenic syndromeEnrichmentCHRNA12.03
26Syndromic intellectual disabilityEnrichmentSYT11.95
27Esophageal atresia/tracheoesophageal fistulaEnrichmentRAB3GAP21.90
28Congenital myopathyEnrichmentCHRNA11.90
29Williams-beuren syndromeEnrichmentSTX1A1.88
30Centronuclear myopathyEnrichmentCHRNA11.86
31Hydrops fetalis, nonimmuneEnrichmentCHRNA11.77
32StrabismusEnrichmentSTXBP11.75
33Non-immune hydrops fetalisEnrichmentCHRNA11.69
34Cystic fibrosisEnrichmentSTX1A1.68
35Optic atrophy plus syndromeEnrichmentSNAP251.54
36West syndromeEnrichmentSTXBP11.54
37Spastic ataxiaEnrichmentSTXBP11.46
38Cone-rod dystrophy 2EnrichmentRIMS11.35

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