Serotonin and anxiety

No Pathway Network information available for Serotonin and anxiety

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

Disorders associated with Serotonin and anxiety SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Developmental and epileptic encephalopathy 91EnrichmentPPP3CA3.05
2Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA3.05
3Periodic fever, menstrual cycle-dependentEnrichmentHTR1A3.05
4Autism 20EnrichmentNLGN13.05
5Undetermined early-onset epileptic encephalopathyEnrichmentGRIN2D, PPP3CA2.97
6Epilepsy, idiopathic generalized 13EnrichmentGABRA12.90
7Spinocerebellar ataxia, autosomal recessive 13EnrichmentGRM12.90
8Intellectual developmental disorder, autosomal dominant 54EnrichmentCAMK2B2.90
9Developmental and epileptic encephalopathy 19EnrichmentGABRA12.90
10Spinocerebellar ataxia 44EnrichmentGRM12.90
11Xq27.3q28 duplication syndromeEnrichmentFMR12.90
12Chondromyxoid fibromaEnrichmentGRM12.90
13Autosomal dominant non-syndromic intellectual disabilityEnrichmentCAMK2B, PPP3CA2.76
14Obsessive-compulsive disorderEnrichmentHTR2A2.75
15Developmental and epileptic encephalopathy 46EnrichmentGRIN2D2.75
16Congenital generalized lipodystrophyEnrichmentFOS2.45
17Obesity, early-onset, with adrenal insufficiency and red hairEnrichmentPOMC2.43
18Obesity due to pro-opiomelanocortin deficiencyEnrichmentPOMC2.43
19Major depressive disorderEnrichmentHTR2A2.35
20Histiocytoid hemangiomaEnrichmentFOS2.35
21Fragile x tremor/ataxia syndromeEnrichmentFMR12.30
22Fragile x-associated tremor/ataxia syndromeEnrichmentFMR12.30
23Premature ovarian failure 1EnrichmentFMR12.20
24Fragile x syndromeEnrichmentFMR12.20
25Childhood absence epilepsyEnrichmentGABRA12.13
26Autosomal dominant sleep-related hypermotor epilepsyEnrichmentCRH2.06
27Dravet syndromeEnrichmentGABRA11.90
28Epilepsy, myoclonic juvenileEnrichmentGABRA11.86
29Epilepsy, idiopathic generalizedEnrichmentGABRA11.86
30DystoniaEnrichmentCAMK2B1.37
31EpilepsyEnrichmentGABRA11.31
32SchizophreniaEnrichmentHTR2A1.29
33Body mass index quantitative trait locus 11EnrichmentPOMC1.22
34Congenital nervous system abnormalityEnrichmentCAMK2B0.90
35Nervous system diseaseEnrichmentCAMK2B0.90
36MicrocephalyEnrichmentCAMK2B0.84

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