Testosterone Enanthate
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB13944 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 86 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | urethral obstruction sequence | KG + DL |
| 2 | tetragametic chimerism | KG + DL |
| 3 | polysomy of X chromosome | KG + DL |
| 4 | testicular regression syndrome | KG + DL |
| 5 | dyschondrosteosis-nephritis syndrome | KG + DL |
| 6 | prune belly syndrome | KG + DL |
| 7 | penile/testicular agenesis | KG + DL |
| 8 | freemartinism | KG + DL |
| 9 | primary ovarian failure | KG + DL |
| 10 | torticollis-keloids-cryptorchidism-renal dysplasia syndrome | KG + DL |
| 11 | 46,XX disorder of sex development-anorectal anomalies syndrome | KG + DL |
| 12 | arthrogryposis epileptic seizures migrational brain disorder | KG + DL |
| 13 | thyrocerebrorenal syndrome | KG + DL |
| 14 | Guttmacher syndrome | KG + DL |
| 15 | Mayer-Rokitansky-Kuster-Hauser syndrome | KG + DL |
| 16 | acropectororenal dysplasia | KG + DL |
| 17 | lower limb deficiency-hypospadias syndrome | KG + DL |
| 18 | inflammatory and autoimmune disease with epilepsy | KG + DL |
| 19 | limb body wall complex | KG + DL |
| 20 | infundibulopelvic stenosis-multicystic kidney syndrome | KG + DL |
| 21 | Mayer-Rokitansky-Küster-Hauser syndrome type 2 | KG + DL |
| 22 | familial omphalocele syndrome with facial dysmorphism | KG + DL |
| 23 | immune epilepsy | KG + DL |
| 24 | caudal regression-sirenomelia spectrum | KG + DL |
| 25 | radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome | KG + DL |
| 26 | symptomatic form of fragile X syndrome in female carrier | KG + DL |
| 27 | pericardial and diaphragmatic defect | KG + DL |
| 28 | trisomy 18 | KG + DL |
| 29 | Juberg-Marsidi syndrome | KG + DL |
| 30 | maternal uniparental disomy of chromosome 16 | KG + DL |
| 31 | axial mesodermal dysplasia spectrum | KG + DL |
| 32 | diaphragmatic defect-limb deficiency-skull defect syndrome | KG + DL |
| 33 | Kleefstra syndrome due to 9q34 microdeletion | KG + DL |
| 34 | cerebral malformation with epilepsy | KG + DL |
| 35 | hydrocephalus-blue sclerae-nephropathy syndrome | KG + DL |
| 36 | ring chromosome 13 | KG + DL |
| 37 | extratemporal epilepsy | KG + DL |
| 38 | structural epilepsy | KG + DL |
| 39 | post-traumatic epilepsy | KG + DL |
| 40 | epilepsia partialis continua | KG + DL |
| 41 | acrorenal syndrome | KG + DL |
| 42 | duplication of urethra | KG + DL |
| 43 | nephrosis-deafness-urinary tract-digital malformations syndrome | KG + DL |
| 44 | oculo-skeletal-renal syndrome | KG + DL |
| 45 | congenital megacalycosis | KG + DL |
| 46 | monosomy 13q34 | KG + DL |
| 47 | distal monosomy 13q | KG + DL |
| 48 | renal nutcracker syndrome | KG + DL |
| 49 | 8p23.1 microdeletion syndrome | KG + DL |
| 50 | Fibulo-ulnar hypoplasia-renal anomalies syndrome | KG + DL |
(Showing top 50 of 86 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.