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 might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Drug repositionability
ID | Diseases (Sorted by drug repositionability) |
---|---|
28 | Systemic amyloidosis |
46 | Malignant rheumatoid arthritis |
51 | Scleroderma |
85 | Idiopathic interstitial pneumonia |
34 | Neurofibromatosis |
2 | Amyotrophic lateral sclerosis |
13 | Multiple sclerosis/Neuromyelitis optica |
49 | Systemic lupus erythematosus |
56 | Behcet disease |
26 | HTLV-1-associated myelopathy |
42 | Polyarteritis nodosa |
65 | Primary immunodeficiency |
96 | Crohn disease |
6 | Parkinson disease |
38 | Stevens-Johnson syndrome |
11 | Myasthenia gravis |
228 | Bronchiolitis obliterans |
331 | Idiopathic multicentric castleman disease |
127 | Frontotemporal lobar degeneration |
86 | Pulmonary arterial hypertension |
93 | Primary biliary cholangitis |
60 | Aplastic anemia |
266 | Familial mediterranean fever |
113 | Muscular dystrophy |
58 | Hypertrophic cardiomyopathy |
107 | Juvenile idiopathic arthritis |
227 | Osler disease |
53 | Sjogren syndrome |
61 | Autoimmune hemolytic anemia |
210 | Single Ventricle |
164 | Oculocutaneous albinism |
283 | Acquired pure red cell aplasia |
97 | Ulcerative colitis |
285 | Fanconi anemia |
36 | Epidermolysis bullosa |
226 | Interstitial cystitis with Hunners ulcer |
162 | Pemphigoid |
41 | Giant cell arteritis |
62 | Paroxysmal nocturnal hemoglobinuria |
284 | Diamond-Blackfan anemia |
35 | Pemphigus |
45 | Eosinophilic granulomatosis with Polyangiitis |
39 | Toxic epidermal necrolysis |
151 | Rasmussen encephalitis |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
20 | Adrenoleukodystrophy |
19 | Lysosomal storage disease |
16 | Crow-Fukase syndrome |
302 | Leber hereditary optic neuropathy |
95 | Autoimmune hepatitis |
222 | Primary nephrotic syndrome |
224 | Purpura nephritis |
66 | IgA nephropathy |
286 | Hereditary sideroblastic anemia |
50 | Dermatomyositis |
84 | Sarcoidosis |
168 | Ehlers-Danlos syndrome |
8 | Huntington disease |
40 | Takayasu arteritis |
70 | Spinal stenosis |
89 | Lymphangioleiomyomatosis |
300 | IgG4-related disease |
269 | Pyogenic arthritis |
256 | Muscle glycogenosis |
64 | Thrombotic thrombocytopenic purpura |
326 | Osteopetrosis |
299 | Cystic fibrosis |
55 | Relapsing polychondritis |
298 | Hereditary pancreatitis |
57 | Idiopathic dilated cardiomyopathy |
63 | Idiopathic thrombocytopenic purpura |
1 | Spinal and bulbar muscular atrophy |
158 | Tuberous sclerosis |
10 | Charcot-Marie-Tooth disease |
25 | Progressive multifocal leukoencephalopathy |
160 | Congenital ichthyosis |
14 | Chronic inflammatory demyelinating polyneuropathy |
87 | Pulmonary veno-occlusive disease |
274 | Osteogenesis Imperfecta |
169 | Menkes disease |
170 | Occipital horn syndrome |
67 | Polycystic kidney disease |
114 | Non-dystrophic myotonia syndrome |
288 | Autoimmune acquired coagulation factor deficiency |
15 | Inclusion body myositis |
193 | Prader-Willi syndrome |
94 | Primary sclerosing cholangitis |
231 | Alpha-1-antitrypsin deficiency |
43 | Microscopic polyangiitis |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
90 | Retinitis pigmentosa |
144 | Lennox-Gastaut syndrome |
118 | Myelomeningocele |
22 | Moyamoya disease |
5 | Progressive supranuclear palsy |
106 | Cryopyrin-associated periodic syndrome |
251 | Urea cycle disorder |
235 | Hypoparathyroidism |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |