Sympathetic Nerve Pathway (Neuroeffector Junction)

No Pathway Network information available for Sympathetic Nerve Pathway (Neuroeffector Junction)

Pathways in the Sympathetic Nerve Pathway (Neuroeffector Junction) SuperPath

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

Disorders associated with Sympathetic Nerve Pathway (Neuroeffector Junction) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizuresEnrichmentCACNA1A, CACNA1C5.08
2Resting heart rate, variation inEnrichmentADRB12.77
3Primary aldosteronism, seizures, and neurologic abnormalitiesEnrichmentCACNA1D2.77
4Brugada syndrome 3EnrichmentCACNA1C2.77
5Sinoatrial node dysfunction and deafnessEnrichmentCACNA1D2.77
6Short sleep, familial natural, 2EnrichmentADRB12.77
7Postural orthostatic tachycardia syndromeEnrichmentSLC6A22.77
8Lipodystrophy, familial partial, type 8EnrichmentADRA2A2.77
9Sporadic hemiplegic migraineEnrichmentCACNA1A2.77
10Atypical timothy syndromeEnrichmentCACNA1C2.77
11Aldosterone-producing adenoma with seizures and neurological abnormalitiesEnrichmentCACNA1D2.77
12Timothy syndrome type 2EnrichmentCACNA1C2.77
13Timothy syndrome type 1EnrichmentCACNA1C2.77
14Cacna1c-related disordersEnrichmentCACNA1C2.77
15Benign paroxysmal torticollis of infancyEnrichmentCACNA1A2.77
16Cerebral palsyEnrichmentCACNA1A, CACNA1C2.71
17N-acetylglutamate synthase deficiencyEnrichmentPYY2.47
18Timothy syndromeEnrichmentCACNA1C2.47
19Alternating hemiplegia of childhood 1EnrichmentCACNA1A2.47
20Orthostatic hypotension 1EnrichmentDBH2.47
21Long qt syndrome 8EnrichmentCACNA1C2.47
22Parkinsonism-dystonia 2, infantile-onsetEnrichmentSLC18A22.47
23Dopamine beta-hydroxylase deficiencyEnrichmentDBH2.47
24Congenital disorder of glycosylation, type iw, autosomal dominantEnrichmentCACNA1D2.47
25Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movementsEnrichmentCACNA1B2.47
26Progressive bulbar palsyEnrichmentCACNA1A2.47
27Undetermined early-onset epileptic encephalopathyEnrichmentCACNA1A, CACNA1B2.40
28Hereditary episodic ataxiaEnrichmentCACNA1A2.29
29Migraine, familial hemiplegic, 1EnrichmentCACNA1A2.17
30Spinocerebellar ataxia 6EnrichmentCACNA1A2.17
31Developmental and epileptic encephalopathy 2EnrichmentCACNA1A2.17
32Ventricular fibrillation, paroxysmal familial, 1EnrichmentCACNA1C2.17
33Developmental and epileptic encephalopathy 42EnrichmentCACNA1A2.17
34Developmental and epileptic encephalopathy 52EnrichmentCACNA1A2.17
35Episodic ataxiaEnrichmentCACNA1A2.17
36Familial or sporadic hemiplegic migraineEnrichmentCACNA1A2.17
37Episodic ataxia, type 2EnrichmentCACNA1A2.07
38Heart conduction diseaseEnrichmentCACNA1C2.07
39Familial adult myoclonic epilepsyEnrichmentADRA2B1.99
40Orthostatic intoleranceEnrichmentSLC6A21.87
41Lennox-gastaut syndromeEnrichmentCACNA1A1.87
42Alternating hemiplegia of childhoodEnrichmentCACNA1A1.87
43Difference of sex developmentEnrichmentCACNA1A1.87
44Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentCACNA1C1.82
45Migraine with or without aura 1EnrichmentCACNA1A1.73
46Cardiac conduction defectEnrichmentCACNA1C1.70
47Cardiomyopathy, familial hypertrophic, 1EnrichmentCACNA1C1.40
48Brugada syndromeEnrichmentCACNA1C1.36
49Auditory neuropathyEnrichmentCACNA1A1.36
50StrabismusEnrichmentCACNA1A1.35
51Long qt syndrome 1EnrichmentCACNA1C1.30
52Long qt syndromeEnrichmentCACNA1C1.29
53Congenital nervous system abnormalityEnrichmentCACNA1A0.78
54Nervous system diseaseEnrichmentCACNA1A0.78
55Complex neurodevelopmental disorderEnrichmentCACNA1C0.72

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