Tolterodine

DrugBank ID: DB01036

Summary

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

Predictions

Indication	Score	Source
overactive bladder (disease)	0.9977	KG+DL
low compliance bladder	0.9631	DL
polycystic kidney disease 3 with or without polycystic liver disease	0.9627	DL
thoracic malformation	0.9594	DL
renal-hepatic-pancreatic dysplasia	0.9577	DL
Joubert syndrome with renal defect	0.9552	DL
adult familial nephronophthisis-spastic quadriparesia syndrome	0.9544	DL
karyomegalic interstitial nephritis	0.9517	DL
congenital analbuminemia	0.9398	DL
hyperamylasemia	0.9332	DL
polyclonal hyperviscosity syndrome	0.9332	DL
polycystic kidney disease	0.9200	DL
blood group incompatibility	0.8841	DL
faciodigitogenital syndrome	0.8706	DL
monoclonal gammopathy	0.8686	DL
attention deficit-hyperactivity disorder	0.8685	DL
premalignant hematological system disease	0.8670	DL
bladder neck obstruction	0.8534	DL
tic disorder	0.8441	DL
communication disorder	0.8401	DL
hematological disease associated with an acquired peripheral neuropathy	0.8347	DL
congenital hematological disorder	0.8305	DL
developmental disorder of mental health	0.8299	DL
fetal nicotine spectrum disorder	0.8280	DL
stereotypic movement disorder	0.8280	DL
transient tic disorder	0.8068	DL
oppositional defiant disorder (disease)	0.7853	DL
Hinman syndrome	0.7765	DL
vesicoureteral reflux	0.7756	DL
postcholecystectomy syndrome	0.7422	DL
urinary system disease	0.7419	DL
detrusor sphincter dyssynergia (disease)	0.7415	DL
female stress incontinence	0.7393	DL
disease of neck of urinary bladder	0.7297	DL
gastroduodenitis	0.7260	DL
familial episodic pain syndrome with predominantly upper body involvement	0.7241	DL
restless legs syndrome	0.7093	DL
Ambras type hypertrichosis universalis congenita	0.6402	DL
septicemic plague	0.6315	DL
hypotrichosis simplex of the scalp	0.6260	DL
polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis	0.6129	DL
epilepsy, juvenile absence, susceptibility to, 1	0.6076	DL
chondromyxoid fibroma	0.6062	DL
Joubert syndrome with hepatic defect	0.6054	DL
syndrome with a Dandy-Walker malformation as major feature	0.5989	DL
sudden arrhythmia death syndrome	0.5977	DL
congenital hypotrichosis milia	0.5939	DL
malformation syndrome with odontal and/or periodontal component	0.5939	DL
Polymerase proofreading-related adenomatous polyposis	0.5938	DL
Duane retraction syndrome 3 with or without deafness	0.5924	DL

External Links

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