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 (DR) might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Score (Drug repositionability)

ID	Diseases (Sorted by score)	Score
271	Ankylosing spondylitis	-
46	Malignant rheumatoid arthritis	39.235
97	Ulcerative colitis	25.078
96	Crohn disease	21.977
107	Juvenile idiopathic arthritis	21.244
13	Multiple sclerosis/Neuromyelitis optica	18.716
50	Dermatomyositis	17.741
51	Scleroderma	17.402
49	Systemic lupus erythematosus	14.940
84	Sarcoidosis	14.540
53	Sjogren syndrome	13.481
162	Pemphigoid	13.410
41	Giant cell arteritis	12.175
65	Primary immunodeficiency	12.033
56	Behcet disease	10.580
40	Takayasu arteritis	9.943
6	Parkinson disease	8.869
11	Myasthenia gravis	8.659
93	Primary biliary cholangitis	8.468
44	Wegener granulomatosis	8.362
299	Cystic fibrosis	6.974
270	Chronic recurrent multifocal osteomyelitis	6.000
298	Hereditary pancreatitis	5.434
222	Primary nephrotic syndrome	5.182
226	Interstitial cystitis with Hunners ulcer	5.104
60	Aplastic anemia	5.059
300	IgG4-related disease	4.995
269	Pyogenic arthritis	4.995
256	Muscle glycogenosis	4.878
55	Relapsing polychondritis	4.581
160	Congenital ichthyosis	4.423
2	Amyotrophic lateral sclerosis	4.104
43	Microscopic polyangiitis	4.098
35	Pemphigus	3.902
19	Lysosomal storage disease	3.535
78	Hypopituitarism	3.412
63	Idiopathic thrombocytopenic purpura	3.380
95	Autoimmune hepatitis	3.334
285	Fanconi anemia	3.278
86	Pulmonary arterial hypertension	3.195
284	Diamond-Blackfan anemia	3.042
66	IgA nephropathy	3.033
265	Lipodystrophy	2.758
42	Polyarteritis nodosa	2.758
8	Huntington disease	2.728
21	Mitochondrial disease	2.657
45	Eosinophilic granulomatosis with Polyangiitis	2.585
113	Muscular dystrophy	2.434
37	Generalised pustular psoriasis	2.415
164	Oculocutaneous albinism	2.390
70	Spinal stenosis	2.341
251	Urea cycle disorder	2.305
85	Idiopathic interstitial pneumonia	2.081
224	Purpura nephritis	2.073
268	Nakajo-Nishimura syndrome	2.000
325	Hereditary autoinflammatory syndrome	2.000
337	Homocystinuria	2.000
257	Hepatic glycogenosis	2.000
282	Congenital dyserythropoietic anemia	2.000
331	Idiopathic multicentric castleman disease	1.869
288	Autoimmune acquired coagulation factor deficiency	1.829
228	Bronchiolitis obliterans	1.809
158	Tuberous sclerosis	1.756
34	Neurofibromatosis	1.662
218	Alport syndrome	1.610
36	Epidermolysis bullosa	1.505
206	Fragile X syndrome	1.447
280	Huge arteriovenous malformation with cervicofacial or limb lesion	1.422
310	Congenital anomalies syndrome	1.366
172	Hypophosphatasia	1.366
225	Congenital nephrogenic diabetes insipidus	1.341
246	Methylmalonic acidemia	1.240
283	Acquired pure red cell aplasia	1.192
94	Primary sclerosing cholangitis	1.150
79	Homozygous familial hypercholesterolemia	1.146
98	Eosinophilic gastrointestinal disease	1.145
236	Pseudohypoparathyroidism	1.112
58	Hypertrophic cardiomyopathy	1.067
333	Hutchinson-Gilford syndrome	1.049
235	Hypoparathyroidism	1.049
71	Idiopathic osteonecrosis of the femoral head	1.049
317	Trifunctional protein deficiency	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