Browse Diseases


Please click on the alphabet below to browse the drugs by the letter of their indicated diseases



Disease DxID Primary Indication Orphan indications* Rare indication Common indication
Dx001150 Darier's disease Tretinoin
Dx000362 Debridement of necrotic tissue Collagenase
Dx000365 Decubitus ulcers Collagenase
Dx000624 Deep venous thrombosis Heparin
Dx001005 Deficiency of argininosuccinic acid synthetase Sodium phenylbutyrate Sodium phenylbutyrate
Dx001003 Deficiency of carbamylphosphate synthetase Sodium phenylbutyrate Sodium phenylbutyrate
Dx001004 Deficiency of ornithine transcarbamylase Sodium phenylbutyrate Sodium phenylbutyrate
Dx000563 Degenerative metabolic bone disease Etidronate disodium
Dx000967 Delayed graft function Recombinant human c1 inhibitor
Dx000741 Deletion 5 q cytogenetic abnormality Lenalidomide
Dx000272 Depression Bupropion; impiramine
Dx000364 Dermal ulcers Collagenase
Dx000447 Dermatitis herpetiformis Dapsone
Dx000518 Dermatomyositis Immuneglobulin intravenous (human) Eculizumab
Dx001129 Desmoid tumor Toremifene
Dx000270 Diabetes mellitus Bromocriptine
Dx000529 Dialysis Levocarnitine Epoetin alfa Levocarnitine
Dx000873 Diarrhea Nitazoxanide Nitazoxanide
Dx000356 Diffuse alveolar hemorrhage Coagulation factor viia (recombinant)
Dx000935 Diffuse large B-cell lymphoma Pralatrexate

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Dudley Laboratory
Department of Genetics and Genomic Sciences
Icahn Institute for Genomics and Multiscale Biology
Icahn School of Medicine at Mount Sinai
One Gustave L. Levy Place, Box 1498
Manhattan, New York City, NY
repurposedb@dudleylab.org