Succinylcholine Pathway, Pharmacokinetics/Pharmacodynamics

No Pathway Network information available for Succinylcholine Pathway, Pharmacokinetics/Pharmacodynamics

Pathways in the Succinylcholine Pathway, Pharmacokinetics/Pharmacodynamics SuperPath

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

Disorders associated with Succinylcholine Pathway, Pharmacokinetics/Pharmacodynamics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Myasthenic syndrome, congenital, 1a, slow-channelEnrichmentCHRNA1, CHRNB1, CHRND, CHRNE10.51
2Postsynaptic congenital myasthenic syndromesEnrichmentCHRNA1, CHRNB1, CHRND, CHRNE9.76
3Centronuclear myopathyEnrichmentCACNA1S, CHRNA1, CHRND, RYR18.68
4Myasthenic syndrome, congenital, 1b, fast-channelEnrichmentCHRNA1, CHRND, CHRNE8.67
5Multiple pterygium syndrome, lethal typeEnrichmentCHRNA1, CHRND, RYR17.53
6Congenital myopathyEnrichmentCACNA1S, CHRNA1, RYR16.29
7Malignant hyperthermiaEnrichmentCACNA1S, RYR15.37
8Congenital myasthenic syndromeEnrichmentCHRNA1, CHRNE4.19
9Fetal akinesia deformation sequence 1EnrichmentCHRND, RYR13.33
10Distal arthrogryposisEnrichmentCHRND, RYR13.22
11Thyrotoxic periodic paralysis 1EnrichmentCACNA1S3.05
12Myasthenic syndrome, congenital, 2a, slow-channelEnrichmentCHRNB13.05
13Myasthenic syndrome, congenital, 2c, associated with acetylcholine receptor deficiencyEnrichmentCHRNB13.05
14Myasthenic syndrome, congenital, 3a, slow-channelEnrichmentCHRND3.05
15Congenital myopathy 18EnrichmentCACNA1S3.05
16Myasthenic syndrome, congenital, 3c, associated with acetylcholine receptor deficiencyEnrichmentCHRND3.05
17Myasthenic syndrome, congenital, 3b, fast-channelEnrichmentCHRND3.05
18Malignant hyperthermia 5EnrichmentCACNA1S3.05
19Developmental and epileptic encephalopathy 110EnrichmentCACNA2D13.05
20Butyrylcholinesterase deficiencyEnrichmentBCHE3.05
21Congenital myopathy with myasthenic-like onsetEnrichmentRYR13.05
22Rhabdomyolysis 2EnrichmentATP2A23.05
23Periodic paralysis with transient compartment-like syndromeEnrichmentCACNA1S3.05
24Calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathyEnrichmentRYR13.05
25Benign samaritan congenital myopathyEnrichmentRYR13.05
26Malignant hyperthermia 1EnrichmentRYR12.75
27Acrokeratosis verruciformisEnrichmentATP2A22.75
28Brody diseaseEnrichmentATP2A12.75
29King-denborough syndromeEnrichmentRYR12.75
30Exercise-induced malignant hyperthermiaEnrichmentRYR12.75
31Darier-white diseaseEnrichmentATP2A22.58
32Lynch syndrome 5EnrichmentRYR12.58
33Bronchopulmonary dysplasiaEnrichmentRYR12.58
34Thyrotoxic periodic paralysisEnrichmentCACNA1S2.58
35Congenital myopathy 1a, autosomal dominant, with malignant hyperthermiaEnrichmentRYR12.45
36Myopathy, centronuclear, 2EnrichmentRYR12.45
37Sacral defect with anterior meningoceleEnrichmentRYR12.45
38Intellectual developmental disorder, autosomal dominant 26EnrichmentRYR12.45
39Congenital myopathy 1aEnrichmentRYR12.45
40Congenital myopathy 1b, autosomal recessiveEnrichmentRYR12.35
41Myasthenic syndrome, congenital, 4a, slow-channelEnrichmentCHRNE2.35
42Cardiac arrestEnrichmentCACNA2D12.35
43Myasthenic syndrome, congenital, 4b, fast-channelEnrichmentCHRNE2.35
44Congenital short qt syndromeEnrichmentCACNA2D12.35
45Hypokalemic periodic paralysis, type 1EnrichmentCACNA1S2.28
46Myopathy, centronuclear, 1EnrichmentRYR12.28
47Brugada syndrome 1EnrichmentCACNA2D12.21
48Congenital muscular dystrophyEnrichmentRYR12.15
49Hydrops fetalisEnrichmentRYR12.10
50Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiencyEnrichmentCHRNE2.05
51Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactylyEnrichmentRYR11.94
52ClubfootEnrichmentRYR11.94
53Congenital myopathy 4a, autosomal dominantEnrichmentRYR11.88
54Arrhythmogenic right ventricular cardiomyopathyEnrichmentRYR11.85
55Beckwith-wiedemann syndromeEnrichmentRYR11.80
56Neuromuscular diseaseEnrichmentRYR11.80
57ScoliosisEnrichmentRYR11.68
58Hydrops fetalis, nonimmuneEnrichmentCHRNA11.64
59Brugada syndromeEnrichmentCACNA2D11.64
60Long qt syndromeEnrichmentCACNA1S1.57
61Non-immune hydrops fetalisEnrichmentCHRNA11.57
62MyopathyEnrichmentRYR11.46
63Undetermined early-onset epileptic encephalopathyEnrichmentCACNA2D11.31
64AutismEnrichmentCHRNA11.21
65Breast cancerEnrichmentCACNA2D11.19

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