296. Biliary atresia Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 73 / Drugs : 67 - (DrugBank : 36) / Drug target genes : 51 - Drug target pathways : 68
Biliary atresia 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 |
|---|---|---|
| 296 | Biliary atresia | - |
| 6 | Parkinson disease | 38.150 |
| 13 | Multiple sclerosis | 36.224 |
| 84 | Sarcoidosis | 23.659 |
| 5 | Progressive supranuclear palsy | 18.162 |
| 22 | Moyamoya disease | 16.825 |
| 98 | Eosinophilic gastro-intestinal disorder | 16.789 |
| 152 | PCDH19 related syndrome | 16.000 |
| 2 | Amyotrophic lateral sclerosis | 15.504 |
| 46 | Malignant rheumatoid arthritis | 15.390 |
| 158 | Tuberous sclerosis | 15.238 |
| 17 | Multiple system atrophy | 14.811 |
| 96 | Crohn disease | 14.400 |
| 18 | Spinocerebellar degeneration | 13.827 |
| 205 | Fragile X syndrome related disease | 13.615 |
| 70 | Spinal stenosis | 13.364 |
| 201 | Angelman syndrome | 13.188 |
| 145 | West syndrome | 13.082 |
| 156 | Rett syndrome | 12.855 |
| 231 | Alpha-1-antitrypsin deficiency | 12.754 |
| 272 | Fibrodysplasia ossificans progressiva | 12.034 |
| 3 | Spinal muscular atrophy | 11.958 |
| 155 | Acquired aphasia with convulsive disorder | 11.378 |
| 36 | Epidermolysis bullosa | 11.167 |
| 298 | Hereditary pancreatitis | 10.868 |
| 97 | Ulcerative colitis | 10.443 |
| 21 | Mitochondrial disease | 10.248 |
| 193 | Prader-Willi syndrome | 9.948 |
| 206 | Fragile X syndrome | 9.752 |
| 8 | Huntington disease | 9.514 |
| 34 | Neurofibromatosis | 9.434 |
| 75 | Cushing disease | 9.323 |
| 140 | Dorabe syndrome | 9.126 |
| 144 | Lennox-Gastaut syndrome | 9.056 |
| 86 | Pulmonary arterial hypertension | 3.603 |
| 53 | Sjogren syndrome | 2.978 |
| 226 | Interstitial cystitis with Hunners ulcer | 2.812 |
| 11 | Myasthenia gravis | 2.592 |
| 299 | Cystic fibrosis | 2.475 |
| 19 | Lysosomal storage disease | 2.185 |
| 26 | HTLV-1-associated myelopathy | 2.178 |
| 297 | Alagille syndrome | 2.000 |
| 338 | Progressive familial intrahepatic cholestasis | 2.000 |
| 278 | Huge lymphatic malformation with cervicofacial lesion | 1.880 |
| 254 | Porphyria | 1.725 |
| 49 | Systemic lupus erythematosus | 1.452 |
| 300 | IgG4-related disease | 1.327 |
| 57 | Idiopathic dilated cardiomyopathy | 1.133 |
| 169 | Menkes disease | 1.133 |
| 170 | Occipital horn syndrome | 1.133 |
| 94 | Primary sclerosing cholangitis | 1.123 |
| 51 | Scleroderma | 1.076 |
| 251 | Urea cycle disorder | 1.044 |
| 167 | Marfan syndrome | 1.040 |
| 35 | Pemphigus | 1.018 |
| 324 | Methylglutaconic aciduria | 1.000 |
| 111 | Congenital myopathy | 1.000 |
| 52 | Mixed connective tissue disease | 1.000 |
| 220 | Rapidly progressive glomerulonephritis | 1.000 |
| 30 | Distal myopathy | 1.000 |