296. Biliary atresia Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 71 / Drugs : 70 - (DrugBank : 39) / Drug target genes : 35 - Drug target pathways : 60
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/Neuromyelitis optica | 36.224 |
84 | Sarcoidosis | 23.659 |
5 | Progressive supranuclear palsy | 18.162 |
22 | Moyamoya disease | 16.825 |
98 | Eosinophilic gastrointestinal disease | 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 |