11. Myasthenia gravis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 332 / Drugs : 234 - (DrugBank : 81) / Drug target genes : 45 - Drug target pathways : 127
Myasthenia gravis 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 |
---|---|---|
11 | Myasthenia gravis | - |
13 | Multiple sclerosis/Neuromyelitis optica | 32.933 |
46 | Malignant rheumatoid arthritis | 31.738 |
96 | Crohn disease | 24.516 |
49 | Systemic lupus erythematosus | 20.020 |
65 | Primary immunodeficiency | 18.194 |
51 | Scleroderma | 17.548 |
6 | Parkinson disease | 15.366 |
53 | Sjogren syndrome | 15.253 |
107 | Juvenile idiopathic arthritis | 14.323 |
40 | Takayasu arteritis | 12.288 |
28 | Systemic amyloidosis | 12.256 |
44 | Wegener granulomatosis | 12.143 |
283 | Acquired pure red cell aplasia | 11.857 |
60 | Aplastic anemia | 11.829 |
284 | Diamond-Blackfan anemia | 11.818 |
164 | Oculocutaneous albinism | 10.541 |
55 | Relapsing polychondritis | 10.307 |
300 | IgG4-related disease | 10.240 |
2 | Amyotrophic lateral sclerosis | 10.181 |
50 | Dermatomyositis | 10.169 |
285 | Fanconi anemia | 10.000 |
61 | Autoimmune hemolytic anemia | 9.756 |
162 | Pemphigoid | 9.545 |
41 | Giant cell arteritis | 9.545 |
62 | Paroxysmal nocturnal hemoglobinuria | 9.478 |
113 | Muscular dystrophy | 9.470 |
222 | Primary nephrotic syndrome | 9.370 |
93 | Primary biliary cholangitis | 9.286 |
85 | Idiopathic interstitial pneumonia | 9.164 |
45 | Eosinophilic granulomatosis with Polyangiitis | 9.067 |
169 | Menkes disease | 9.000 |
170 | Occipital horn syndrome | 9.000 |
256 | Muscle glycogenosis | 8.711 |
14 | Chronic inflammatory demyelinating polyneuropathy | 8.704 |
271 | Ankylosing spondylitis | 8.659 |
42 | Polyarteritis nodosa | 8.378 |
286 | Hereditary sideroblastic anemia | 8.000 |
97 | Ulcerative colitis | 7.680 |
95 | Autoimmune hepatitis | 7.501 |
226 | Interstitial cystitis with Hunners ulcer | 7.344 |
66 | IgA nephropathy | 7.189 |
19 | Lysosomal storage disease | 7.174 |
43 | Microscopic polyangiitis | 6.429 |
228 | Bronchiolitis obliterans | 6.400 |
118 | Myelomeningocele | 6.261 |
224 | Purpura nephritis | 6.120 |
269 | Pyogenic arthritis | 6.120 |
22 | Moyamoya disease | 5.954 |
234 | Peroxisomal disease (except Adrenoleukodystrophy) | 5.807 |
35 | Pemphigus | 5.758 |
70 | Spinal stenosis | 5.576 |
288 | Autoimmune acquired coagulation factor deficiency | 5.400 |
84 | Sarcoidosis | 5.221 |
26 | HTLV-1-associated myelopathy | 5.095 |
12 | Congenital myasthenic syndrome | 5.000 |
302 | Leber hereditary optic neuropathy | 5.000 |
5 | Progressive supranuclear palsy | 4.825 |
64 | Thrombotic thrombocytopenic purpura | 4.711 |
326 | Osteopetrosis | 4.711 |
58 | Hypertrophic cardiomyopathy | 4.594 |
158 | Tuberous sclerosis | 4.444 |
56 | Behcet disease | 4.383 |
57 | Idiopathic dilated cardiomyopathy | 4.267 |
151 | Rasmussen encephalitis | 4.259 |
331 | Idiopathic multicentric castleman disease | 3.890 |
38 | Stevens-Johnson syndrome | 3.847 |
20 | Adrenoleukodystrophy | 3.814 |
36 | Epidermolysis bullosa | 3.810 |
227 | Osler disease | 3.710 |
39 | Toxic epidermal necrolysis | 3.636 |
86 | Pulmonary arterial hypertension | 3.603 |
17 | Multiple system atrophy | 3.497 |
160 | Congenital ichthyosis | 3.388 |
4 | Primary lateral sclerosis | 3.267 |
90 | Retinitis pigmentosa | 3.122 |
34 | Neurofibromatosis | 3.116 |
299 | Cystic fibrosis | 3.032 |
274 | Osteogenesis Imperfecta | 3.029 |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion | 3.029 |
3 | Spinal muscular atrophy | 3.023 |
323 | Aromatic L-amino acid decarboxylase deficiency | 3.000 |
206 | Fragile X syndrome | 3.000 |
127 | Frontotemporal lobar degeneration | 2.738 |
63 | Idiopathic thrombocytopenic purpura | 2.592 |
296 | Biliary atresia | 2.592 |
215 | Tetralogy of Fallot | 2.533 |
210 | Single Ventricle | 2.382 |
251 | Urea cycle disorder | 2.300 |
8 | Huntington disease | 2.049 |
78 | Hypopituitarism | 2.029 |
268 | Nakajo-Nishimura syndrome | 2.000 |
325 | Hereditary autoinflammatory syndrome | 2.000 |
337 | Homocystinuria | 2.000 |
278 | Huge lymphatic malformation with cervicofacial lesion | 1.880 |
16 | Crow-Fukase syndrome | 1.880 |
94 | Primary sclerosing cholangitis | 1.725 |
270 | Chronic recurrent multifocal osteomyelitis | 1.600 |
25 | Progressive multifocal leukoencephalopathy | 1.400 |
172 | Hypophosphatasia | 1.363 |
212 | Tricuspid atresia | 1.250 |
254 | Porphyria | 1.123 |
167 | Marfan syndrome | 1.040 |
21 | Mitochondrial disease | 1.028 |
111 | Congenital myopathy | 1.000 |
54 | Adult still disease | 1.000 |
52 | Mixed connective tissue disease | 1.000 |
220 | Rapidly progressive glomerulonephritis | 1.000 |
30 | Distal myopathy | 1.000 |