Melatonin
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB01065 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 100 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | insomnia (disease) | DL |
| 2 | sleep disorder, initiating and maintaining sleep | DL |
| 3 | migraine with brainstem aura | KG + DL |
| 4 | obesity disorder | KG + DL |
| 5 | restless legs syndrome | KG + DL |
| 6 | migraine disorder | KG + DL |
| 7 | hypervitaminosis | KG + DL |
| 8 | obsolete hypertelorism (disease) | KG + DL |
| 9 | monogenic obesity | KG + DL |
| 10 | frontorhiny | KG + DL |
| 11 | proximal 16p11.2 microdeletion syndrome | KG + DL |
| 12 | acute encephalopathy with biphasic seizures and late reduced diffusion | KG + DL |
| 13 | fibrosis of extraocular muscles, congenital, with synergistic divergence | KG + DL |
| 14 | hypercarotenemia and vitamin A deficiency, autosomal recessive | KG + DL |
| 15 | hyperparathyroidism, primary, caused by water clear cell hyperplasia | KG + DL |
| 16 | retinal aplasia | KG + DL |
| 17 | melanoma, malignant familial intraocular | KG + DL |
| 18 | atrophoderma vermiculata | KG + DL |
| 19 | sella turcica, bridged | KG + DL |
| 20 | triphalangeal thumb, Nonopposable | KG + DL |
| 21 | hypospadias 3, autosomal | KG + DL |
| 22 | mitral valve prolapse, myxomatous | KG + DL |
| 23 | sclerocornea, autosomal dominant | KG + DL |
| 24 | myoglobinuria, recurrent | KG + DL |
| 25 | abdominal obesity-metabolic syndrome quantitative trait locus 2 | KG + DL |
| 26 | hemangiomas of small intestine | KG + DL |
| 27 | glaucoma with elevated episcleral venous pressure | KG + DL |
| 28 | hyperemesis gravidarum (disease) | KG + DL |
| 29 | macular dystrophy, fenestrated sheen type | KG + DL |
| 30 | trichotillomania | KG + DL |
| 31 | postural orthostatic tachycardia syndrome | KG + DL |
| 32 | ACys amyloidosis | KG + DL |
| 33 | diarrhea 11, malabsorptive, congenital | KG + DL |
| 34 | cholangiocarcinoma, susceptibility to | KG + DL |
| 35 | Tukel syndrome | KG + DL |
| 36 | hereditary persistence of alpha-fetoprotein | KG + DL |
| 37 | sinus node disease and myopia | KG + DL |
| 38 | pancreas, dorsal, agenesis of | KG + DL |
| 39 | astigmatism (disease) | KG + DL |
| 40 | ulerythema ophryogenesis | KG + DL |
| 41 | spinal chordoma | KG + DL |
| 42 | epilepsy, childhood absence, susceptibility to | KG + DL |
| 43 | sudden arrhythmia death syndrome | KG + DL |
| 44 | lattice degeneration of retina leading to retinal detachment | KG + DL |
| 45 | celiac artery stenosis from compression by median arcuate ligament of diaphragm | KG + DL |
| 46 | Blount disease, infantile | KG + DL |
| 47 | hernia, anterior diaphragmatic | KG + DL |
| 48 | ovarian fibroma (disease) | KG + DL |
| 49 | vas deferens, congenital bilateral aplasia of, X-linked | KG + DL |
| 50 | familial chronic myelocytic leukemia-like syndrome | KG + DL |
(Showing top 50 of 100 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.