Melatonin metabolism and effects

No Pathway Network information available for Melatonin metabolism and effects

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

Disorders associated with Melatonin metabolism and effects SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Advanced sleep phase syndromeEnrichmentPER2, PER34.82
2Drug metabolism, poor, cyp2c19-relatedEnrichmentCYP2C192.64
3Advanced sleep phase syndrome, familial, 1EnrichmentPER22.64
4Resting heart rate, variation inEnrichmentADRB12.64
5Yt blood group antigenEnrichmentACHE2.64
6Advanced sleep phase syndrome, familial, 3EnrichmentPER32.64
7Auriculocondylar syndrome 3EnrichmentEDN12.64
8Intellectual developmental disorder, autosomal recessive 63EnrichmentCAMK2A2.64
9Question mark ears, isolatedEnrichmentEDN12.64
10Drug metabolism, poor, cyp2d6-relatedEnrichmentCYP2D62.64
11Hirschsprung disease, cardiac defects, and autonomic dysfunctionEnrichmentECE12.64
12Delayed sleep phase disorderEnrichmentCRY12.64
13Short sleep, familial natural, 2EnrichmentADRB12.64
14Intellectual developmental disorder, autosomal dominant 53EnrichmentCAMK2A2.64
15Glaucoma 1, open angle, aEnrichmentCYP1B12.34
16Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM12.34
17Homocystinuria-megaloblastic anemia, cble typeEnrichmentPER32.34
18Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.34
19Long qt syndrome 14EnrichmentCALM12.34
20Anterior segment dysgenesis 6EnrichmentCYP1B12.34
21Primary congenital glaucomaEnrichmentCYP1B12.34
22Common variable immunodeficiency 12EnrichmentNFKB12.34
23Auriculocondylar syndrome 1EnrichmentEDN12.04
24Glaucoma 3, primary infantile, bEnrichmentCYP1B12.04
25Pediatric systemic lupus erythematosusEnrichmentIRAK12.04
26Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.94
27Rhabdomyosarcoma 2EnrichmentFOXO11.94
28Juvenile glaucomaEnrichmentCYP1B11.94
29Glaucoma, primary open angleEnrichmentCYP1B11.87
30Anterior segment dysgenesis 5EnrichmentCYP1B11.87
31Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.87
32Glaucoma 3, primary congenital, aEnrichmentCYP1B11.80
33Common variable immunodeficiencyEnrichmentNFKB11.80
34Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.74
35Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM11.74
36Peters-plus syndromeEnrichmentCYP1B11.65
37Ciliary dyskinesia, primary, 3EnrichmentNFKB11.65
38Anterior segment dysgenesisEnrichmentCYP1B11.47
39Hypertension, essentialEnrichmentECE11.42
40Diffuse large b-cell lymphomaEnrichmentFOXO11.37
41Hirschsprung disease 1EnrichmentECE11.19
42Long qt syndrome 1EnrichmentCALM11.18
43Long qt syndromeEnrichmentCALM11.16
44Systemic lupus erythematosusEnrichmentIRAK11.07
45Type 2 diabetes mellitusEnrichmentMTNR1B1.04
46Autosomal dominant non-syndromic intellectual disabilityEnrichmentCAMK2A0.97

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