Tolvaptan

DrugBank ID: DB06212

Summary

Metric	Value
Total Predictions	51
KG+DL (Dual Validated)	2
DL Only	48
KG Only	1

Predictions

Indication	Score	Source
polycystic kidney disease 3 with or without polycystic liver disease	0.9999	DL
renal-hepatic-pancreatic dysplasia	0.9998	DL
karyomegalic interstitial nephritis	0.9998	DL
thoracic malformation	0.9998	DL
polycystic kidney disease	0.9998	KG+DL
Joubert syndrome with renal defect	0.9998	DL
adult familial nephronophthisis-spastic quadriparesia syndrome	0.9998	DL
Ambras type hypertrichosis universalis congenita	0.9996	DL
hypertrichosis (disease)	0.9996	DL
malformation syndrome with odontal and/or periodontal component	0.9996	DL
syndrome with a Dandy-Walker malformation as major feature	0.9995	DL
isolated genetic hair shaft abnormality	0.9995	DL
nephrogenic syndrome of inappropriate antidiuresis	0.9994	KG+DL
homozygous familial hypercholesterolemia	0.9987	DL
Joubert syndrome with oculorenal defect	0.9984	DL
Meckel syndrome,	0.9984	DL
syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy	0.9981	DL
hypoalphalipoproteinemia	0.9979	DL
autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis	0.9974	DL
congenital pulmonary lymphangiectasia	0.9963	DL
multiple endocrine neoplasia	0.9963	DL
polycystic liver disease	0.9961	DL
16q24.1 microdeletion syndrome	0.9960	DL
primary interstitial lung disease specific to childhood	0.9958	DL
congenital alveolar capillary dysplasia	0.9958	DL
isolated pulmonary capillaritis	0.9957	DL
cranioectodermal dysplasia	0.9953	DL
RHYNS syndrome	0.9952	DL
gastrocutaneous syndrome	0.9949	DL
nephrogenic diabetes insipidus	0.9945	DL
familial generalized lentiginosis	0.9943	DL
psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome	0.9942	DL
Joubert syndrome with hepatic defect	0.9941	DL
Senior-Boichis syndrome	0.9939	DL
renal tubule disease	0.9938	DL
isolated encephalocele	0.9938	DL
Moynahan syndrome	0.9935	DL
sitosterolemia	0.9934	DL
acromelanosis	0.9933	DL
congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome	0.9933	DL
pulmonary arterial hypertension	0.9932	DL
osteopathia striata-pigmentary dermopathy-white forelock syndrome	0.9931	DL
pulmonary arteriovenous malformation (disease)	0.9930	DL
rhabdoid tumor	0.9929	DL
pulmonary arterial hypertension associated with congenital heart disease	0.9928	DL
renal fibrosis	0.9927	DL
dermatofibrosarcoma protuberans	0.9926	DL
laterality defects, autosomal dominant	0.9926	DL
familial caudal dysgenesis	0.9924	DL
leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome	0.9923	DL

Showing top 50 of 51 predictions.

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