Nicotine Pathway (Dopaminergic Neuron), Pharmacodynamics

No Pathway Network information available for Nicotine Pathway (Dopaminergic Neuron), Pharmacodynamics

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

Disorders associated with Nicotine Pathway (Dopaminergic Neuron), Pharmacodynamics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Smoking as a quantitative trait locus 3EnrichmentCHRNA3, CHRNA55.64
2Epilepsy, nocturnal frontal lobe, 1EnrichmentCHRNA4, CHRNB25.16
3Autosomal dominant nocturnal frontal lobe epilepsyEnrichmentCHRNA4, CHRNB24.86
4Autosomal dominant sleep-related hypermotor epilepsyEnrichmentCHRNA4, CHRNB24.32
5Presynaptic congenital myasthenic syndromesEnrichmentSNAP25, VAMP13.20
6DystoniaEnrichmentGNB1, TH2.88
7Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary cakutEnrichmentCHRNA32.81
8Tremor, hereditary essential, 1EnrichmentDRD32.81
9Lissencephaly 7 with cerebellar hypoplasiaEnrichmentCDK52.81
10Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalitiesEnrichmentGNAI12.81
11Epilepsy, nocturnal frontal lobe, 3EnrichmentCHRNB22.81
12Pulmonary hypertension, primary, 4EnrichmentKCNK32.81
13Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.81
14Cardioacrofacial dysplasia 1EnrichmentPRKACA2.81
15Intellectual developmental disorder, autosomal dominant 42EnrichmentGNB12.81
16Autonomic nervous system diseaseEnrichmentDRD42.81
17Segawa syndrome, autosomal recessiveEnrichmentTH2.51
18Birk-barel syndromeEnrichmentKCNK92.51
19Aromatic l-amino acid decarboxylase deficiencyEnrichmentDDC2.51
20Parkinsonism-dystonia 2, infantile-onsetEnrichmentSLC18A22.51
21Fibrolamellar carcinomaEnrichmentPRKACA2.51
22Cerebral visual impairmentEnrichmentGNB12.51
23Diarrhea 12, with microvillus atrophyEnrichmentSTX32.46
24Developmental and epileptic encephalopathy 117EnrichmentSNAP252.46
25Hemophagocytic lymphohistiocytosis, familial, 4EnrichmentSTX112.46
26Congenital disorder of glycosylation, type iiaaEnrichmentSTX52.46
27Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movementsEnrichmentVAMP22.46
28Deafness, autosomal recessive 123EnrichmentSTX42.46
29Epilepsy with generalized tonic-clonic seizuresEnrichmentSNAP252.46
30Retinal dystrophy and microvillus inclusion diseaseEnrichmentSTX32.46
31Generalized epilepsy with febrile seizures plus, type 9EnrichmentSTX1B2.46
32Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCHRNA3, CHRNA42.45
33Dystonia, dopa-responsiveEnrichmentTH2.33
34Tobacco addictionEnrichmentCHRNA42.21
35Spastic ataxia 1, autosomal dominantEnrichmentVAMP12.16
36Spastic ataxia 1EnrichmentVAMP12.16
37Myasthenic syndrome, congenital, 25, presynapticEnrichmentVAMP12.16
38Dystonia 11, myoclonicEnrichmentDRD22.03
39Microvillus inclusion diseaseEnrichmentSTX31.98
40HypothyroidismEnrichmentGNB11.91
41Essential tremorEnrichmentDRD31.91
42Pseudohypoparathyroidism, type ibEnrichmentSTX161.86
43Developmental and epileptic encephalopathy 2EnrichmentSNAP251.86
44Generalized epilepsyEnrichmentSTX1B1.86
45Ellis-van creveld syndromeEnrichmentPRKACA1.86
46Frontotemporal dementia 1EnrichmentCHRNA41.77
47Leukemia, acute lymphoblasticEnrichmentGNB11.77
48Myelodysplastic syndromeEnrichmentGNB11.77
49Heritable pulmonary arterial hypertensionEnrichmentKCNK31.77
50Hemophagocytic lymphohistiocytosis, familial, 1EnrichmentSTX111.76
51Pulmonary hypertension, primary, 1EnrichmentKCNK31.70
52Focal epilepsyEnrichmentSNAP251.62
53Cleft palate, isolatedEnrichmentGNB11.58
54Attention deficit-hyperactivity disorderEnrichmentDRD41.47
55RasopathyEnrichmentDDC1.40
56StrabismusEnrichmentGNB11.39
57Stereotypic movement disorderEnrichmentSNAP251.36
58Generalized epilepsy with febrile seizures plusEnrichmentSTX1B1.32
59Congenital myasthenic syndromeEnrichmentVAMP11.32
60Cerebral palsyEnrichmentGNB11.23
61Williams-beuren syndromeEnrichmentSTX1A1.17
62MicrocephalyEnrichmentGNB1, SNAP251.17
63Autosomal dominant non-syndromic intellectual disabilityEnrichmentGNB11.13
64SchizophreniaEnrichmentDRD31.06
65Cystic fibrosisEnrichmentSTX1A0.98
66Developmental and epileptic encephalopathyEnrichmentSNAP250.93
67Optic atrophy plus syndromeEnrichmentSNAP250.85
68Sensorineural hearing lossEnrichmentSTX40.81
69Autism spectrum disorderEnrichmentGNB10.81
70AutismEnrichmentSTX1A0.65

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