231. Alpha-1-antitrypsin deficiency Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 93 / Drugs : 77 - (DrugBank : 8) / Drug target genes : 10 - Drug target pathways : 36
Alpha-1-antitrypsin deficiency 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 |
---|---|---|
231 | Alpha-1-antitrypsin deficiency | - |
6 | Parkinson disease | 29.724 |
97 | Ulcerative colitis | 28.225 |
13 | Multiple sclerosis/Neuromyelitis optica | 26.198 |
70 | Spinal stenosis | 23.353 |
96 | Crohn disease | 23.333 |
298 | Hereditary pancreatitis | 22.594 |
46 | Malignant rheumatoid arthritis | 21.729 |
2 | Amyotrophic lateral sclerosis | 20.325 |
36 | Epidermolysis bullosa | 20.152 |
34 | Neurofibromatosis | 17.199 |
140 | Dorabe syndrome | 16.275 |
22 | Moyamoya disease | 16.208 |
144 | Lennox-Gastaut syndrome | 16.200 |
193 | Prader-Willi syndrome | 16.059 |
152 | PCDH19 related syndrome | 16.000 |
158 | Tuberous sclerosis | 15.029 |
156 | Rett syndrome | 14.891 |
84 | Sarcoidosis | 14.751 |
8 | Huntington disease | 14.700 |
201 | Angelman syndrome | 13.631 |
3 | Spinal muscular atrophy | 13.428 |
75 | Cushing disease | 12.976 |
205 | Fragile X syndrome related disease | 12.873 |
5 | Progressive supranuclear palsy | 12.853 |
296 | Biliary atresia | 12.754 |
272 | Fibrodysplasia ossificans progressiva | 12.659 |
21 | Mitochondrial disease | 12.605 |
145 | West syndrome | 12.461 |
206 | Fragile X syndrome | 12.171 |
155 | Acquired aphasia with convulsive disorder | 12.106 |
98 | Eosinophilic gastrointestinal disease | 10.704 |
17 | Multiple system atrophy | 10.694 |
18 | Spinocerebellar degeneration | 10.403 |
10 | Charcot-Marie-Tooth disease | 6.317 |
107 | Juvenile idiopathic arthritis | 5.934 |
1 | Spinal and bulbar muscular atrophy | 4.011 |
226 | Interstitial cystitis with Hunners ulcer | 3.973 |
256 | Muscle glycogenosis | 3.421 |
168 | Ehlers-Danlos syndrome | 3.095 |
86 | Pulmonary arterial hypertension | 2.916 |
51 | Scleroderma | 2.847 |
113 | Muscular dystrophy | 2.665 |
58 | Hypertrophic cardiomyopathy | 2.217 |
38 | Stevens-Johnson syndrome | 2.143 |
53 | Sjogren syndrome | 2.113 |
337 | Homocystinuria | 2.000 |
114 | Non-dystrophic myotonia syndrome | 1.905 |
28 | Systemic amyloidosis | 1.481 |
127 | Frontotemporal lobar degeneration | 1.250 |
251 | Urea cycle disorder | 1.057 |
111 | Congenital myopathy | 1.000 |