3. Spinal muscular atrophy Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 237 / Drugs : 123 - (DrugBank : 29) / Drug target genes : 51 - Drug target pathways : 75
Spinal muscular atrophy 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 |
---|---|---|
3 | Spinal muscular atrophy | - |
13 | Multiple sclerosis/Neuromyelitis optica | 45.983 |
6 | Parkinson disease | 41.411 |
2 | Amyotrophic lateral sclerosis | 38.440 |
5 | Progressive supranuclear palsy | 37.572 |
206 | Fragile X syndrome | 28.157 |
18 | Spinocerebellar degeneration | 26.997 |
17 | Multiple system atrophy | 24.672 |
97 | Ulcerative colitis | 23.421 |
156 | Rett syndrome | 23.313 |
8 | Huntington disease | 22.881 |
205 | Fragile X syndrome related disease | 20.456 |
193 | Prader-Willi syndrome | 19.507 |
140 | Dorabe syndrome | 18.671 |
144 | Lennox-Gastaut syndrome | 18.531 |
46 | Malignant rheumatoid arthritis | 17.926 |
70 | Spinal stenosis | 16.795 |
21 | Mitochondrial disease | 16.352 |
152 | PCDH19 related syndrome | 16.000 |
96 | Crohn disease | 15.883 |
34 | Neurofibromatosis | 15.588 |
22 | Moyamoya disease | 15.082 |
158 | Tuberous sclerosis | 14.663 |
145 | West syndrome | 14.038 |
203 | 22q11.2 deletion syndrome | 14.000 |
231 | Alpha-1-antitrypsin deficiency | 13.428 |
201 | Angelman syndrome | 12.954 |
296 | Biliary atresia | 11.958 |
272 | Fibrodysplasia ossificans progressiva | 11.704 |
298 | Hereditary pancreatitis | 11.181 |
155 | Acquired aphasia with convulsive disorder | 10.993 |
98 | Eosinophilic gastrointestinal disease | 10.241 |
75 | Cushing disease | 9.564 |
36 | Epidermolysis bullosa | 8.477 |
127 | Frontotemporal lobar degeneration | 8.278 |
84 | Sarcoidosis | 7.847 |
102 | Rubinstein-Taybi syndrome | 7.000 |
85 | Idiopathic interstitial pneumonia | 6.635 |
256 | Muscle glycogenosis | 5.376 |
215 | Tetralogy of Fallot | 5.264 |
4 | Primary lateral sclerosis | 5.068 |
12 | Congenital myasthenic syndrome | 5.000 |
233 | Wolfram syndrome | 4.791 |
65 | Primary immunodeficiency | 4.606 |
113 | Muscular dystrophy | 4.605 |
78 | Hypopituitarism | 4.462 |
89 | Lymphangioleiomyomatosis | 4.019 |
222 | Primary nephrotic syndrome | 3.217 |
49 | Systemic lupus erythematosus | 3.124 |
11 | Myasthenia gravis | 3.023 |
331 | Idiopathic multicentric castleman disease | 2.960 |
26 | HTLV-1-associated myelopathy | 2.638 |
14 | Chronic inflammatory demyelinating polyneuropathy | 2.358 |
90 | Retinitis pigmentosa | 2.317 |
251 | Urea cycle disorder | 2.292 |
86 | Pulmonary arterial hypertension | 2.201 |
337 | Homocystinuria | 2.000 |
76 | Pituitary gonadotropin secretion hyperthyroidism | 1.585 |
1 | Spinal and bulbar muscular atrophy | 1.019 |
299 | Cystic fibrosis | 1.012 |
111 | Congenital myopathy | 1.000 |
191 | Werner syndrome | 1.000 |
220 | Rapidly progressive glomerulonephritis | 1.000 |
30 | Distal myopathy | 1.000 |