151. Rasmussen encephalitis Disease details / Clinical trials / Drug dev / DR info
Clinical trial : 1 / Drugs : 2 - (DrugBank : 1) / Drug target genes : 5 - Drug target pathways : 33
Rasmussen encephalitis and other diseases between which drug repositioning (DR) might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Score (Drug repositionability)
| ID | Diseases (Sorted by score) | Score |
|---|---|---|
| 151 | Rasmussen encephalitis | - |
| 226 | Interstitial cystitis with Hunners ulcer | 6.000 |
| 269 | Pyogenic arthritis | 6.000 |
| 42 | Polyarteritis nodosa | 6.000 |
| 45 | Eosinophilic granulomatosis with Polyangiitis | 6.000 |
| 55 | Relapsing polychondritis | 6.000 |
| 95 | Autoimmune hepatitis | 6.000 |
| 284 | Diamond-Blackfan anemia | 6.000 |
| 13 | Multiple sclerosis/Neuromyelitis optica | 6.000 |
| 20 | Adrenoleukodystrophy | 6.000 |
| 2 | Amyotrophic lateral sclerosis | 6.000 |
| 39 | Toxic epidermal necrolysis | 6.000 |
| 160 | Congenital ichthyosis | 6.000 |
| 19 | Lysosomal storage disease | 6.000 |
| 46 | Malignant rheumatoid arthritis | 6.000 |
| 49 | Systemic lupus erythematosus | 6.000 |
| 51 | Scleroderma | 6.000 |
| 60 | Aplastic anemia | 6.000 |
| 65 | Primary immunodeficiency | 6.000 |
| 85 | Idiopathic interstitial pneumonia | 6.000 |
| 96 | Crohn disease | 6.000 |
| 222 | Primary nephrotic syndrome | 6.000 |
| 285 | Fanconi anemia | 6.000 |
| 53 | Sjogren syndrome | 6.000 |
| 26 | HTLV-1-associated myelopathy | 6.000 |
| 28 | Systemic amyloidosis | 6.000 |
| 162 | Pemphigoid | 6.000 |
| 228 | Bronchiolitis obliterans | 6.000 |
| 227 | Osler disease | 6.000 |
| 38 | Stevens-Johnson syndrome | 6.000 |
| 50 | Dermatomyositis | 6.000 |
| 56 | Behcet disease | 6.000 |
| 107 | Juvenile idiopathic arthritis | 6.000 |
| 97 | Ulcerative colitis | 6.000 |
| 58 | Hypertrophic cardiomyopathy | 6.000 |
| 164 | Oculocutaneous albinism | 6.000 |
| 40 | Takayasu arteritis | 6.000 |
| 41 | Giant cell arteritis | 6.000 |
| 302 | Leber hereditary optic neuropathy | 5.000 |
| 286 | Hereditary sideroblastic anemia | 4.688 |
| 234 | Peroxisomal disease (except Adrenoleukodystrophy) | 4.514 |
| 274 | Osteogenesis Imperfecta | 4.464 |
| 224 | Purpura nephritis | 4.444 |
| 64 | Thrombotic thrombocytopenic purpura | 4.427 |
| 326 | Osteopetrosis | 4.427 |
| 283 | Acquired pure red cell aplasia | 4.398 |
| 62 | Paroxysmal nocturnal hemoglobinuria | 4.365 |
| 61 | Autoimmune hemolytic anemia | 4.333 |
| 66 | IgA nephropathy | 4.286 |
| 158 | Tuberous sclerosis | 4.286 |
| 93 | Primary biliary cholangitis | 4.286 |
| 11 | Myasthenia gravis | 4.259 |
| 63 | Idiopathic thrombocytopenic purpura | 4.259 |
| 36 | Epidermolysis bullosa | 4.252 |
| 90 | Retinitis pigmentosa | 4.252 |
| 113 | Muscular dystrophy | 4.237 |
| 299 | Cystic fibrosis | 4.210 |
| 6 | Parkinson disease | 4.189 |