GABA receptor signaling

No Pathway Network information available for GABA receptor signaling

Pathways in the GABA receptor signaling SuperPath

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

Disorders associated with GABA receptor signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Hypocalciuric hypercalcemia, familial, type iiiEnrichmentAP2S13.02
2Neurodevelopmental disorder with poor language and loss of hand skillsEnrichmentGABBR23.02
3Developmental and epileptic encephalopathy 59EnrichmentGABBR23.02
4Gaba aminotransferase deficiencyEnrichmentABAT3.02
5Gaba-transaminase deficiencyEnrichmentABAT3.02
6Generalized epilepsy with febrile seizures plus, type 12EnrichmentSLC32A13.02
7Neurodevelopmental disorder with language delay and variable cognitive abnormalitiesEnrichmentGABBR13.02
8Developmental and epileptic encephalopathy 114EnrichmentSLC32A13.02
9Hyperekplexia 1EnrichmentGPHN2.72
10Retinal dystrophy, juvenile cataracts, and short stature syndromeEnrichmentGPHN2.72
11Molybdenum cofactor deficiency, type cEnrichmentGPHN2.72
12Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentAP2M12.72
13Leber congenital amaurosis 13EnrichmentGPHN2.54
14Glycosylphosphatidylinositol biosynthesis defect 17EnrichmentGPHN2.54
15Arachnoid cystEnrichmentGPHN2.54
16Tobacco addictionEnrichmentGABBR22.42
17Macular dystrophy with or without cone dysfunctionEnrichmentGPHN2.42
18HyperekplexiaEnrichmentGPHN2.32
19AnxietyEnrichmentGPHN2.24
20Rett syndromeEnrichmentGABBR22.17
21Rett syndrome, congenital variantEnrichmentGABBR22.12
22Neurofibromatosis, type iEnrichmentGABBR12.07
23Myoclonic-atonic epilepsyEnrichmentAP2M12.07
24Generalized epilepsy with febrile seizures plusEnrichmentSLC32A11.87
25Early infantile developmental and epileptic encephalopathyEnrichmentSLC32A11.77
26Stargardt disease 1EnrichmentGPHN1.55
27Eye diseaseEnrichmentGPHN1.48
28Cerebral palsyEnrichmentGPHN1.43
29Autosomal dominant non-syndromic intellectual disabilityEnrichmentGABBR11.33
30Undetermined early-onset epileptic encephalopathyEnrichmentGABBR21.28
31Cone-rod dystrophy 2EnrichmentGPHN1.20
32Leber plus diseaseEnrichmentGPHN1.06
33Retinitis pigmentosaEnrichmentGPHN0.73
34Hereditary retinal dystrophyEnrichmentGPHN0.61
35Fundus dystrophyEnrichmentGPHN0.61

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