271. Ankylosing spondylitis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 574 / Drugs : 359 - (DrugBank : 68) / Drug target genes : 41 - Drug target pathways : 146
Ankylosing spondylitis 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) |
---|---|
271 | Ankylosing spondylitis |
46 | Malignant rheumatoid arthritis |
97 | Ulcerative colitis |
96 | Crohn disease |
107 | Juvenile idiopathic arthritis |
13 | Multiple sclerosis/Neuromyelitis optica |
50 | Dermatomyositis |
51 | Scleroderma |
49 | Systemic lupus erythematosus |
84 | Sarcoidosis |
53 | Sjogren syndrome |
162 | Pemphigoid |
41 | Giant cell arteritis |
65 | Primary immunodeficiency |
56 | Behcet disease |
40 | Takayasu arteritis |
6 | Parkinson disease |
11 | Myasthenia gravis |
93 | Primary biliary cholangitis |
44 | Wegener granulomatosis |
299 | Cystic fibrosis |
270 | Chronic recurrent multifocal osteomyelitis |
298 | Hereditary pancreatitis |
222 | Primary nephrotic syndrome |
226 | Interstitial cystitis with Hunners ulcer |
60 | Aplastic anemia |
300 | IgG4-related disease |
269 | Pyogenic arthritis |
256 | Muscle glycogenosis |
55 | Relapsing polychondritis |
160 | Congenital ichthyosis |
2 | Amyotrophic lateral sclerosis |
43 | Microscopic polyangiitis |
35 | Pemphigus |
19 | Lysosomal storage disease |
78 | Hypopituitarism |
63 | Idiopathic thrombocytopenic purpura |
95 | Autoimmune hepatitis |
285 | Fanconi anemia |
86 | Pulmonary arterial hypertension |
284 | Diamond-Blackfan anemia |
66 | IgA nephropathy |
265 | Lipodystrophy |
42 | Polyarteritis nodosa |
8 | Huntington disease |
21 | Mitochondrial disease |
45 | Eosinophilic granulomatosis with Polyangiitis |
113 | Muscular dystrophy |
37 | Generalised pustular psoriasis |
164 | Oculocutaneous albinism |
70 | Spinal stenosis |
251 | Urea cycle disorder |
85 | Idiopathic interstitial pneumonia |
224 | Purpura nephritis |
268 | Nakajo-Nishimura syndrome |
325 | Hereditary autoinflammatory syndrome |
337 | Homocystinuria |
257 | Hepatic glycogenosis |
282 | Congenital dyserythropoietic anemia |
331 | Idiopathic multicentric castleman disease |
288 | Autoimmune acquired coagulation factor deficiency |
228 | Bronchiolitis obliterans |
158 | Tuberous sclerosis |
34 | Neurofibromatosis |
218 | Alport syndrome |
36 | Epidermolysis bullosa |
206 | Fragile X syndrome |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
310 | Congenital anomalies syndrome |
172 | Hypophosphatasia |
225 | Congenital nephrogenic diabetes insipidus |
246 | Methylmalonic acidemia |
283 | Acquired pure red cell aplasia |
94 | Primary sclerosing cholangitis |
79 | Homozygous familial hypercholesterolemia |
98 | Eosinophilic gastrointestinal disease |
236 | Pseudohypoparathyroidism |
58 | Hypertrophic cardiomyopathy |
333 | Hutchinson-Gilford syndrome |
235 | Hypoparathyroidism |
71 | Idiopathic osteonecrosis of the femoral head |
317 | Trifunctional protein deficiency |
54 | Adult still disease |
52 | Mixed connective tissue disease |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |