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.



Disclaimer
Predictions are for research purposes only and do not constitute medical advice.

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