Testosterone
DrugBank ID: DB00624
Summary
| Metric | Value |
|---|---|
| Total Predictions | 74 |
| KG+DL (Dual Validated) | 5 |
| DL Only | 45 |
| KG Only | 24 |
Predictions
| Indication | Score | Source |
|---|---|---|
| androgen insensitivity syndrome | 0.9750 | KG+DL |
| polysomy of X chromosome | 0.9488 | DL |
| tetragametic chimerism | 0.9466 | DL |
| penile/testicular agenesis | 0.9462 | DL |
| hypogonadotropic hypogonadism with or without anosmia | 0.9449 | KG+DL |
| testicular regression syndrome | 0.9446 | DL |
| Leydig cell hypoplasia due to LH resistance | 0.9424 | DL |
| urethral obstruction sequence | 0.9418 | DL |
| 46,XX disorder of sex development-anorectal anomalies syndrome | 0.9415 | DL |
| freemartinism | 0.9403 | DL |
| arthrogryposis epileptic seizures migrational brain disorder | 0.9384 | DL |
| primary ovarian failure | 0.9373 | DL |
| Mayer-Rokitansky-Kuster-Hauser syndrome | 0.9370 | DL |
| blepharophimosis-epicanthus inversus-ptosis | 0.9370 | DL |
| hydrocephalus-blue sclerae-nephropathy syndrome | 0.9368 | DL |
| inflammatory and autoimmune disease with epilepsy | 0.9368 | DL |
| Guttmacher syndrome | 0.9362 | DL |
| cryptorchidism (disease) | 0.9361 | KG+DL |
| Kleefstra syndrome due to 9q34 microdeletion | 0.9355 | DL |
| cerebral malformation with epilepsy | 0.9350 | DL |
| lower limb deficiency-hypospadias syndrome | 0.9350 | DL |
| prune belly syndrome | 0.9350 | DL |
| immune epilepsy | 0.9349 | DL |
| torticollis-keloids-cryptorchidism-renal dysplasia syndrome | 0.9347 | DL |
| symptomatic form of fragile X syndrome in female carrier | 0.9347 | DL |
| Mayer-Rokitansky-Küster-Hauser syndrome type 2 | 0.9346 | DL |
| 46,XY disorder of sex development due to impaired androgen production | 0.9338 | DL |
| acrorenal syndrome | 0.9337 | DL |
| limb body wall complex | 0.9332 | DL |
| nephrosis-deafness-urinary tract-digital malformations syndrome | 0.9331 | DL |
| trisomy 13 | 0.9330 | KG+DL |
| pericardial and diaphragmatic defect | 0.9329 | DL |
| diaphragmatic defect-limb deficiency-skull defect syndrome | 0.9323 | DL |
| acropectororenal dysplasia | 0.9323 | DL |
| trisomy 18 | 0.9322 | DL |
| Juberg-Marsidi syndrome | 0.9322 | DL |
| radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome | 0.9319 | DL |
| axial mesodermal dysplasia spectrum | 0.9316 | DL |
| dyschondrosteosis-nephritis syndrome | 0.9315 | DL |
| maternal uniparental disomy of chromosome 16 | 0.9315 | DL |
| epilepsia partialis continua | 0.9312 | DL |
| extratemporal epilepsy | 0.9312 | DL |
| post-traumatic epilepsy | 0.9312 | DL |
| structural epilepsy | 0.9312 | DL |
| caudal regression-sirenomelia spectrum | 0.9312 | DL |
| ring chromosome 13 | 0.9311 | DL |
| duplication of urethra | 0.9310 | DL |
| infundibulopelvic stenosis-multicystic kidney syndrome | 0.9309 | DL |
| familial omphalocele syndrome with facial dysmorphism | 0.9307 | DL |
| short stature due to growth hormone qualitative anomaly | 0.9300 | KG+DL |
Showing top 50 of 74 predictions.
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.