28. Systemic amyloidosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 267 / Drugs : 241 - (DrugBank : 77) / Drug target genes : 68 - Drug target pathways : 180
Systemic amyloidosis 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 |
---|---|---|
28 | Systemic amyloidosis | - |
46 | Malignant rheumatoid arthritis | 32.822 |
51 | Scleroderma | 26.066 |
85 | Idiopathic interstitial pneumonia | 25.587 |
34 | Neurofibromatosis | 22.759 |
2 | Amyotrophic lateral sclerosis | 20.774 |
13 | Multiple sclerosis/Neuromyelitis optica | 19.622 |
49 | Systemic lupus erythematosus | 17.943 |
56 | Behcet disease | 16.296 |
26 | HTLV-1-associated myelopathy | 15.825 |
42 | Polyarteritis nodosa | 15.357 |
65 | Primary immunodeficiency | 14.795 |
96 | Crohn disease | 13.610 |
6 | Parkinson disease | 13.337 |
38 | Stevens-Johnson syndrome | 13.265 |
11 | Myasthenia gravis | 12.256 |
228 | Bronchiolitis obliterans | 12.050 |
331 | Idiopathic multicentric castleman disease | 11.300 |
127 | Frontotemporal lobar degeneration | 10.800 |
86 | Pulmonary arterial hypertension | 10.560 |
93 | Primary biliary cholangitis | 10.509 |
60 | Aplastic anemia | 9.487 |
266 | Familial mediterranean fever | 9.036 |
113 | Muscular dystrophy | 8.903 |
58 | Hypertrophic cardiomyopathy | 8.849 |
107 | Juvenile idiopathic arthritis | 8.505 |
227 | Osler disease | 8.461 |
53 | Sjogren syndrome | 8.280 |
61 | Autoimmune hemolytic anemia | 7.989 |
210 | Single Ventricle | 7.795 |
164 | Oculocutaneous albinism | 7.512 |
283 | Acquired pure red cell aplasia | 7.435 |
97 | Ulcerative colitis | 7.267 |
285 | Fanconi anemia | 7.084 |
36 | Epidermolysis bullosa | 6.957 |
226 | Interstitial cystitis with Hunners ulcer | 6.909 |
162 | Pemphigoid | 6.673 |
41 | Giant cell arteritis | 6.673 |
62 | Paroxysmal nocturnal hemoglobinuria | 6.635 |
284 | Diamond-Blackfan anemia | 6.417 |
35 | Pemphigus | 6.417 |
45 | Eosinophilic granulomatosis with Polyangiitis | 6.229 |
39 | Toxic epidermal necrolysis | 6.083 |
151 | Rasmussen encephalitis | 6.000 |
234 | Peroxisomal disease (except Adrenoleukodystrophy) | 5.657 |
20 | Adrenoleukodystrophy | 5.372 |
19 | Lysosomal storage disease | 5.208 |
16 | Crow-Fukase syndrome | 5.000 |
302 | Leber hereditary optic neuropathy | 5.000 |
95 | Autoimmune hepatitis | 4.909 |
222 | Primary nephrotic syndrome | 4.785 |
224 | Purpura nephritis | 4.719 |
66 | IgA nephropathy | 4.714 |
286 | Hereditary sideroblastic anemia | 4.636 |
50 | Dermatomyositis | 4.636 |
84 | Sarcoidosis | 4.216 |
168 | Ehlers-Danlos syndrome | 4.182 |
8 | Huntington disease | 4.176 |
40 | Takayasu arteritis | 4.025 |
70 | Spinal stenosis | 3.967 |
89 | Lymphangioleiomyomatosis | 3.818 |
300 | IgG4-related disease | 3.663 |
269 | Pyogenic arthritis | 3.663 |
256 | Muscle glycogenosis | 3.484 |
64 | Thrombotic thrombocytopenic purpura | 3.480 |
326 | Osteopetrosis | 3.480 |
299 | Cystic fibrosis | 3.409 |
55 | Relapsing polychondritis | 3.273 |
298 | Hereditary pancreatitis | 3.116 |
57 | Idiopathic dilated cardiomyopathy | 2.946 |
63 | Idiopathic thrombocytopenic purpura | 2.782 |
1 | Spinal and bulbar muscular atrophy | 2.689 |
158 | Tuberous sclerosis | 2.577 |
10 | Charcot-Marie-Tooth disease | 2.479 |
25 | Progressive multifocal leukoencephalopathy | 2.390 |
160 | Congenital ichthyosis | 2.364 |
14 | Chronic inflammatory demyelinating polyneuropathy | 2.304 |
87 | Pulmonary veno-occlusive disease | 2.284 |
274 | Osteogenesis Imperfecta | 2.029 |
169 | Menkes disease | 1.912 |
170 | Occipital horn syndrome | 1.912 |
67 | Polycystic kidney disease | 1.895 |
114 | Non-dystrophic myotonia syndrome | 1.662 |
288 | Autoimmune acquired coagulation factor deficiency | 1.662 |
15 | Inclusion body myositis | 1.609 |
193 | Prader-Willi syndrome | 1.601 |
94 | Primary sclerosing cholangitis | 1.595 |
231 | Alpha-1-antitrypsin deficiency | 1.481 |
43 | Microscopic polyangiitis | 1.316 |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion | 1.316 |
90 | Retinitis pigmentosa | 1.213 |
144 | Lennox-Gastaut syndrome | 1.213 |
118 | Myelomeningocele | 1.210 |
22 | Moyamoya disease | 1.204 |
5 | Progressive supranuclear palsy | 1.049 |
106 | Cryopyrin-associated periodic syndrome | 1.030 |
251 | Urea cycle disorder | 1.030 |
235 | Hypoparathyroidism | 1.030 |
220 | Rapidly progressive glomerulonephritis | 1.000 |
30 | Distal myopathy | 1.000 |