Finasteride

DrugBank ID: DB01216

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	1
DL Only	49
KG Only	0

Predictions

Indication	Score	Source
Ambras type hypertrichosis universalis congenita	0.9999	DL
hypertrichosis (disease)	0.9999	DL
malformation syndrome with odontal and/or periodontal component	0.9999	DL
syndrome with a Dandy-Walker malformation as major feature	0.9999	DL
benign prostatic hyperplasia (disease)	0.9999	KG+DL
isolated genetic hair shaft abnormality	0.9999	DL
familial isolated trichomegaly	0.9915	DL
prostate calculus	0.9860	DL
persistent fetal circulation syndrome	0.9049	DL
chronic thromboembolic pulmonary hypertension	0.8987	DL
migraine with brainstem aura	0.8884	DL
pulmonary arterial hypertension associated with congenital heart disease	0.8860	DL
pulmonary arteriovenous malformation (disease)	0.8840	DL
obsolete patella aplasia, coxa vara, and tarsal synostosis	0.8694	DL
pulmonary arterial hypertension	0.8677	DL
kyphoscoliotic heart disease	0.8671	DL
pulmonary arterial hypertension associated with HIV infection	0.8669	DL
pulmonary arterial hypertension associated with chronic hemolytic anemia	0.8669	DL
pulmonary arterial hypertension associated with connective tissue disease	0.8669	DL
pulmonary arterial hypertension associated with schistosomiasis	0.8669	DL
genetic alopecia	0.8645	DL
familial clubfoot due to 17q23.1q23.2 microduplication	0.8611	DL
pulmonary hypertension, primary, autosomal recessive	0.8532	DL
syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy	0.8413	DL
coxopodopatellar syndrome	0.8376	DL
chromosome 17q23.1-q23.2 deletion syndrome	0.8344	DL
migraine disorder	0.8318	DL
allergic urticaria	0.8290	DL
pulmonary hypertension	0.8146	DL
hypotrichosis simplex of the scalp	0.7825	DL
congenital hypotrichosis milia	0.7650	DL
prostatitis (disease)	0.7216	DL
diffuse alopecia areata	0.6961	DL
alopecia	0.6541	DL
trigeminal autonomic cephalalgia	0.6515	DL
mitral valve prolapse, myxomatous	0.6468	DL
nasopharyngitis	0.6334	DL
pulmonary hypertension, primary	0.6265	DL
hyperparathyroidism, primary, caused by water clear cell hyperplasia	0.6101	DL
16q24.1 microdeletion syndrome	0.5962	DL
sudden arrhythmia death syndrome	0.5921	DL
isolated pulmonary capillaritis	0.5844	DL
hypospadias 3, autosomal	0.5811	DL
sella turcica, bridged	0.5811	DL
triphalangeal thumb, Nonopposable	0.5811	DL
primary interstitial lung disease specific to childhood	0.5811	DL
idiopathic pulmonary arterial hypertension	0.5776	DL
fibrosis of extraocular muscles, congenital, with synergistic divergence	0.5752	DL
melanoma, malignant familial intraocular	0.5745	DL
congenital cystic eye multiple ocular and intracranial anomalies	0.5709	DL

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