Benzodiazepine Pathway, Pharmacodynamics

No Pathway Network information available for Benzodiazepine Pathway, Pharmacodynamics

Pathways in the Benzodiazepine Pathway, Pharmacodynamics SuperPath

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

Disorders associated with Benzodiazepine Pathway, Pharmacodynamics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Childhood absence epilepsyEnrichmentGABRA1, GABRG24.83
2Dravet syndromeEnrichmentGABRA1, GABRG24.35
3Generalized epilepsy with febrile seizures plusEnrichmentGABRG2, SLC32A14.05
4Slc6a1-related neurodevelopmental disorderEnrichmentSLC6A13.23
5Benign epilepsy with centrotemporal spikesEnrichmentGABRG2, SLC6A13.10
6Centralopathic epilepsyEnrichmentGABRG2, SLC6A13.06
7Developmental and epileptic encephalopathy 94EnrichmentSLC6A13.05
8Febrile seizures, familial, 8EnrichmentGABRG22.99
9Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 2EnrichmentSLC25A42.99
10Epilepsy, idiopathic generalized 13EnrichmentGABRA12.99
11Mitochondrial dna depletion syndrome 12b , autosomal recessiveEnrichmentSLC25A42.99
12Dystonia 22, adult-onsetEnrichmentTSPOAP12.99
13Developmental and epileptic encephalopathy 74EnrichmentGABRG22.99
14Mitochondrial dna depletion syndrome 12a , autosomal dominantEnrichmentSLC25A42.99
15Developmental and epileptic encephalopathy 19EnrichmentGABRA12.99
16Generalized epilepsy with febrile seizures plus, type 12EnrichmentSLC32A12.99
17Mitochondrial metabolism diseaseEnrichmentSLC25A42.99
18Developmental and epileptic encephalopathy 92EnrichmentGABRB22.99
19Developmental and epileptic encephalopathy 114EnrichmentSLC32A12.99
20Undetermined early-onset epileptic encephalopathyEnrichmentGABRB2, GABRG22.83
21Segawa syndrome, autosomal recessiveEnrichmentTSPOAP12.69
22Dystonia 22, juvenile-onsetEnrichmentTSPOAP12.69
23Myoclonic-atonic epilepsyEnrichmentSLC6A12.58
24Sengers syndromeEnrichmentSLC25A42.51
25Autosomal dominant nocturnal frontal lobe epilepsyEnrichmentGABRG22.38
26Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1EnrichmentSLC25A42.21
27Lennox-gastaut syndromeEnrichmentGABRG22.08
28Epilepsy, myoclonic juvenileEnrichmentGABRA11.95
29Epilepsy, idiopathic generalizedEnrichmentGABRA11.95
30Mitochondrial myopathyEnrichmentSLC25A41.95
31Autosomal dominant non-syndromic intellectual disabilityEnrichmentSLC6A11.83
32MyopiaEnrichmentSLC25A41.81
33Early infantile developmental and epileptic encephalopathyEnrichmentSLC32A11.73
34EpilepsyEnrichmentGABRA11.39
35Bardet-biedl syndromeEnrichmentTSPOAP11.37
36Hypertrophic cardiomyopathyEnrichmentSLC25A41.36
37SchizophreniaEnrichmentGABRB21.23
38Mitochondrial diseaseEnrichmentSLC25A41.06

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