228. Bronchiolitis obliterans Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 97 / Drugs : 118 - (DrugBank : 32) / Drug target genes : 33 - Drug target pathways : 156
Bronchiolitis obliterans and other diseases between which drug repositioning might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Drug repositionability
ID | Diseases (Sorted by drug repositionability) |
---|---|
228 | Bronchiolitis obliterans |
85 | Idiopathic interstitial pneumonia |
51 | Scleroderma |
46 | Malignant rheumatoid arthritis |
13 | Multiple sclerosis/Neuromyelitis optica |
227 | Osler disease |
28 | Systemic amyloidosis |
50 | Dermatomyositis |
222 | Primary nephrotic syndrome |
65 | Primary immunodeficiency |
164 | Oculocutaneous albinism |
49 | Systemic lupus erythematosus |
60 | Aplastic anemia |
162 | Pemphigoid |
283 | Acquired pure red cell aplasia |
107 | Juvenile idiopathic arthritis |
39 | Toxic epidermal necrolysis |
269 | Pyogenic arthritis |
96 | Crohn disease |
41 | Giant cell arteritis |
53 | Sjogren syndrome |
66 | IgA nephropathy |
61 | Autoimmune hemolytic anemia |
11 | Myasthenia gravis |
38 | Stevens-Johnson syndrome |
84 | Sarcoidosis |
285 | Fanconi anemia |
34 | Neurofibromatosis |
284 | Diamond-Blackfan anemia |
151 | Rasmussen encephalitis |
56 | Behcet disease |
45 | Eosinophilic granulomatosis with Polyangiitis |
2 | Amyotrophic lateral sclerosis |
89 | Lymphangioleiomyomatosis |
95 | Autoimmune hepatitis |
58 | Hypertrophic cardiomyopathy |
62 | Paroxysmal nocturnal hemoglobinuria |
224 | Purpura nephritis |
20 | Adrenoleukodystrophy |
93 | Primary biliary cholangitis |
302 | Leber hereditary optic neuropathy |
326 | Osteopetrosis |
6 | Parkinson disease |
19 | Lysosomal storage disease |
40 | Takayasu arteritis |
42 | Polyarteritis nodosa |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
36 | Epidermolysis bullosa |
97 | Ulcerative colitis |
35 | Pemphigus |
64 | Thrombotic thrombocytopenic purpura |
63 | Idiopathic thrombocytopenic purpura |
299 | Cystic fibrosis |
55 | Relapsing polychondritis |
113 | Muscular dystrophy |
286 | Hereditary sideroblastic anemia |
226 | Interstitial cystitis with Hunners ulcer |
158 | Tuberous sclerosis |
26 | HTLV-1-associated myelopathy |
160 | Congenital ichthyosis |
274 | Osteogenesis Imperfecta |
268 | Nakajo-Nishimura syndrome |
325 | Hereditary autoinflammatory syndrome |
276 | Achondroplasia |
16 | Crow-Fukase syndrome |
86 | Pulmonary arterial hypertension |
271 | Ankylosing spondylitis |
44 | Wegener granulomatosis |
90 | Retinitis pigmentosa |
43 | Microscopic polyangiitis |
256 | Muscle glycogenosis |
331 | Idiopathic multicentric castleman disease |
300 | IgG4-related disease |
98 | Eosinophilic gastrointestinal disease |
94 | Primary sclerosing cholangitis |
106 | Cryopyrin-associated periodic syndrome |
235 | Hypoparathyroidism |
15 | Inclusion body myositis |
111 | Congenital myopathy |
108 | TNF receptor-associated periodic syndrome |
267 | Hyper-IgD syndrome |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |
137 | Focal cortical dysplasia |
192 | Cockayne syndrome |
277 | Lymphangiomatosis |
281 | Klippel-Trenaunay-Weber syndrome |