Postsynaptic nicotinic acetylcholine receptors

Pathway network for the Postsynaptic nicotinic acetylcholine receptors SuperPath

Sources:
  • Reactome

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

Disorders associated with Postsynaptic nicotinic acetylcholine receptors SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Myasthenic syndrome, congenital, 1b, fast-channelEnrichmentCHRNA1, CHRND, CHRNE8.67
2Autosomal dominant sleep-related hypermotor epilepsyEnrichmentCHRNA2, CHRNA4, CHRNB28.15
3Myasthenic syndrome, congenital, 1a, slow-channelEnrichmentCHRNA1, CHRND, CHRNE7.73
4Multiple pterygium syndrome, lethal typeEnrichmentCHRNA1, CHRND, CHRNG7.53
5Postsynaptic congenital myasthenic syndromesEnrichmentCHRNA1, CHRND, CHRNE6.94
6Smoking as a quantitative trait locus 3EnrichmentCHRNA3, CHRNA56.41
7Epilepsy, nocturnal frontal lobe, 1EnrichmentCHRNA4, CHRNB26.16
8Autosomal dominant nocturnal frontal lobe epilepsyEnrichmentCHRNA4, CHRNB25.86
9Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCHRNA3, CHRNA4, CHRNB45.59
10Frontotemporal dementia 1EnrichmentCHRNA4, CHRNB44.90
11Congenital myasthenic syndromeEnrichmentCHRNA1, CHRNE4.19
12Centronuclear myopathyEnrichmentCHRNA1, CHRND3.83
13Fetal akinesia deformation sequence 1EnrichmentCHRND, CHRNG3.82
14Distal arthrogryposisEnrichmentCHRND, CHRNG3.71
15Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary cakutEnrichmentCHRNA33.29
16Myasthenic syndrome, congenital, 3a, slow-channelEnrichmentCHRND3.29
17Myasthenic syndrome, congenital, 3c, associated with acetylcholine receptor deficiencyEnrichmentCHRND3.29
18Epilepsy, nocturnal frontal lobe, 3EnrichmentCHRNB23.29
19Myasthenic syndrome, congenital, 3b, fast-channelEnrichmentCHRND3.29
20Epilepsy, nocturnal frontal lobe, 4EnrichmentCHRNA23.18
21Multiple pterygium syndrome, escobar variantEnrichmentCHRNG2.81
22Chromosome 15q13.3 deletion syndromeEnrichmentCHRNA72.75
23Tobacco addictionEnrichmentCHRNA42.69
24Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1bEnrichmentCHRNG2.69
25Myasthenic syndrome, congenital, 4a, slow-channelEnrichmentCHRNE2.59
26Myasthenic syndrome, congenital, 4b, fast-channelEnrichmentCHRNE2.59
27Rheumatoid arthritisEnrichmentCHRNG2.33
28Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiencyEnrichmentCHRNE2.29
29Pulmonary disease, chronic obstructiveEnrichmentCHRNB42.17
30ScoliosisEnrichmentCHRNG1.91
31Congenital myopathyEnrichmentCHRNA11.90
32Peripheral nervous system diseaseEnrichmentCHRNG1.79
33NeuropathyEnrichmentCHRNG1.79
34Hydrops fetalis, nonimmuneEnrichmentCHRNA11.77
35Non-immune hydrops fetalisEnrichmentCHRNA11.69
36AutismEnrichmentCHRNA11.33

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