Lacidipine

DrugBank ID: DB09236

Summary

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

Predictions

Indication	Score	Source
migraine disorder	0.9834	DL
nephrogenic syndrome of inappropriate antidiuresis	0.9820	DL
migraine with brainstem aura	0.9807	DL
pulmonary hypertension	0.9789	DL
kyphoscoliotic heart disease	0.9761	DL
alopecia	0.9737	DL
Prinzmetal angina	0.9733	DL
Raynaud disease	0.9728	DL
hypotrichosis simplex of the scalp	0.9713	DL
congenital hypotrichosis milia	0.9690	DL
open-angle glaucoma	0.9655	DL
primary hereditary glaucoma	0.9648	DL
diffuse alopecia areata	0.9647	DL
benign prostatic hyperplasia (disease)	0.9629	DL
congestive heart failure	0.9551	DL
headache disorder	0.9541	DL
trigeminal autonomic cephalalgia	0.9486	DL
acute pulmonary heart disease	0.9484	DL
cor pulmonale	0.9451	DL
hypertrichosis (disease)	0.9447	DL
chronic pulmonary heart disease	0.9416	DL
hypertensive disorder	0.9391	DL
malformation syndrome with odontal and/or periodontal component	0.9368	DL
subarachnoid hemorrhage (disease)	0.9367	DL
pseudopelade of Brocq	0.9363	DL
Ambras type hypertrichosis universalis congenita	0.9354	DL
syndrome with a Dandy-Walker malformation as major feature	0.9348	DL
pulmonary hypertension owing to lung disease and/or hypoxia	0.9334	DL
pulmonary hypertension with unclear multifactorial mechanism	0.9334	DL
isolated genetic hair shaft abnormality	0.9309	DL
malignant hypertensive renal disease	0.9306	DL
malignant renovascular hypertension	0.9306	DL
atrophoderma vermiculata	0.9289	DL
peripheral vascular disease	0.9243	DL
Braddock syndrome	0.9233	DL
pulmonary hypertension, primary, autosomal recessive	0.9232	DL
cerebrovascular disorder	0.9222	DL
ulerythema ophryogenesis	0.9220	DL
migraine with or without aura, susceptibility to	0.9206	DL
nephrogenic diabetes insipidus	0.9180	DL
obsolete patella aplasia, coxa vara, and tarsal synostosis	0.9178	DL
Moyomoya angiopathy	0.9131	DL
idiopathic macular telangiectasia	0.9089	DL
vasoproliferative tumor of retina	0.9089	DL
intracranial arteriosclerosis	0.9023	DL
benign choroid plexus neoplasm	0.9020	DL
IRVAN syndrome	0.8997	DL
familial clubfoot due to 17q23.1q23.2 microduplication	0.8988	DL
androgenetic alopecia	0.8982	DL
chromosome 17q23.1-q23.2 deletion syndrome	0.8965	DL

External Links

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