Sympathetic Nerve Pathway (Pre- and Post- Ganglionic Junction)

No Pathway Network information available for Sympathetic Nerve Pathway (Pre- and Post- Ganglionic Junction)

Pathways in the Sympathetic Nerve Pathway (Pre- and Post- Ganglionic Junction) SuperPath

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

Disorders associated with Sympathetic Nerve Pathway (Pre- and Post- Ganglionic Junction) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Presynaptic congenital myasthenic syndromesEnrichmentCHAT, SLC18A3, SLC5A77.06
2Myasthenic syndrome, congenital, 21, presynapticEnrichmentCHAT, SLC18A36.14
3Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizuresEnrichmentCACNA1A, CACNA1C5.67
4Cerebral palsyEnrichmentCACNA1A, CACNA1C3.28
5Neuronopathy, distal hereditary motor, autosomal dominant 7EnrichmentSLC5A73.05
6Apnea, central sleepEnrichmentCHAT3.05
7Yt blood group antigenEnrichmentACHE3.05
8Primary aldosteronism, seizures, and neurologic abnormalitiesEnrichmentCACNA1D3.05
9Brugada syndrome 3EnrichmentCACNA1C3.05
10Sinoatrial node dysfunction and deafnessEnrichmentCACNA1D3.05
11Developmental and epileptic encephalopathy 69EnrichmentCACNA1E3.05
12Aspiration pneumoniaEnrichmentCHAT3.05
13Sporadic hemiplegic migraineEnrichmentCACNA1A3.05
14Atypical timothy syndromeEnrichmentCACNA1C3.05
15Aldosterone-producing adenoma with seizures and neurological abnormalitiesEnrichmentCACNA1D3.05
16Timothy syndrome type 2EnrichmentCACNA1C3.05
17Timothy syndrome type 1EnrichmentCACNA1C3.05
18Cacna1c-related disordersEnrichmentCACNA1C3.05
19Benign paroxysmal torticollis of infancyEnrichmentCACNA1A3.05
20Undetermined early-onset epileptic encephalopathyEnrichmentCACNA1A, CACNA1B2.97
21Timothy syndromeEnrichmentCACNA1C2.75
22Alternating hemiplegia of childhood 1EnrichmentCACNA1A2.75
23Segawa syndrome, autosomal recessiveEnrichmentTH2.75
24Aromatic l-amino acid decarboxylase deficiencyEnrichmentDDC2.75
25Long qt syndrome 8EnrichmentCACNA1C2.75
26Myasthenic syndrome, congenital, 20, presynapticEnrichmentSLC5A72.75
27Chromosome 15q13.3 deletion syndromeEnrichmentCHRNA72.75
28Congenital disorder of glycosylation, type iw, autosomal dominantEnrichmentCACNA1D2.75
29Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movementsEnrichmentCACNA1B2.75
30Distal hereditary motor neuropathy type 7EnrichmentSLC5A72.75
31Progressive bulbar palsyEnrichmentCACNA1A2.75
32Van der woude syndrome 1EnrichmentCACNA1E2.58
33Dystonia, dopa-responsiveEnrichmentTH2.58
34Myasthenic syndrome, congenital, 6, presynapticEnrichmentCHAT2.58
35Bronchopulmonary dysplasiaEnrichmentCHAT2.58
36Hereditary episodic ataxiaEnrichmentCACNA1A2.58
37Migraine, familial hemiplegic, 1EnrichmentCACNA1A2.45
38Spinocerebellar ataxia 6EnrichmentCACNA1A2.45
39Developmental and epileptic encephalopathy 2EnrichmentCACNA1A2.45
40Ventricular fibrillation, paroxysmal familial, 1EnrichmentCACNA1C2.45
41Developmental and epileptic encephalopathy 42EnrichmentCACNA1A2.45
42Developmental and epileptic encephalopathy 52EnrichmentCACNA1A2.45
43Episodic ataxiaEnrichmentCACNA1A2.45
44Familial or sporadic hemiplegic migraineEnrichmentCACNA1A2.45
45Episodic ataxia, type 2EnrichmentCACNA1A2.35
46Heart conduction diseaseEnrichmentCACNA1C2.35
47Gastroesophageal refluxEnrichmentCHAT2.15
48Lennox-gastaut syndromeEnrichmentCACNA1A2.15
49Alternating hemiplegia of childhoodEnrichmentCACNA1A2.15
50Difference of sex developmentEnrichmentCACNA1A2.15
51Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentCACNA1C2.10
52Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiencyEnrichmentCHAT2.05
53Migraine with or without aura 1EnrichmentCACNA1A2.01
54Cardiac conduction defectEnrichmentCACNA1C1.98
55Lactic acidosisEnrichmentCHAT1.98
56Congenital myasthenic syndromeEnrichmentCHAT1.91
57Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentSLC5A71.78
58Cardiomyopathy, familial hypertrophic, 1EnrichmentCACNA1C1.68
59Brugada syndromeEnrichmentCACNA1C1.64
60RasopathyEnrichmentDDC1.64
61Auditory neuropathyEnrichmentCACNA1A1.64
62StrabismusEnrichmentCACNA1A1.63
63Long qt syndrome 1EnrichmentCACNA1C1.58
64Long qt syndromeEnrichmentCACNA1C1.57
65DystoniaEnrichmentTH1.52
66Developmental and epileptic encephalopathyEnrichmentCACNA1E1.50
67Fetal akinesia deformation sequence 1EnrichmentSLC18A31.49
68Congenital nervous system abnormalityEnrichmentCACNA1A1.05
69Nervous system diseaseEnrichmentCACNA1A1.05
70Complex neurodevelopmental disorderEnrichmentCACNA1C0.98

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