DR info

Clinical trials : 194 / Drugs : 244 - (DrugBank : 89) / Drug target genes : 50 - Drug target pathways : 151

Dermatomyositis 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
50	Dermatomyositis	-
46	Malignant rheumatoid arthritis	33.229
13	Multiple sclerosis/Neuromyelitis optica	31.214
97	Ulcerative colitis	29.266
96	Crohn disease	28.929
51	Scleroderma	24.354
107	Juvenile idiopathic arthritis	22.615
41	Giant cell arteritis	22.096
49	Systemic lupus erythematosus	21.711
84	Sarcoidosis	21.581
56	Behcet disease	20.000
271	Ankylosing spondylitis	17.741
162	Pemphigoid	16.705
53	Sjogren syndrome	16.030
65	Primary immunodeficiency	15.200
40	Takayasu arteritis	13.487
269	Pyogenic arthritis	13.339
93	Primary biliary cholangitis	12.536
55	Relapsing polychondritis	12.000
228	Bronchiolitis obliterans	11.677
222	Primary nephrotic syndrome	11.096
164	Oculocutaneous albinism	10.353
11	Myasthenia gravis	10.169
60	Aplastic anemia	9.397
284	Diamond-Blackfan anemia	9.122
226	Interstitial cystitis with Hunners ulcer	8.937
2	Amyotrophic lateral sclerosis	8.789
285	Fanconi anemia	8.711
95	Autoimmune hepatitis	8.684
6	Parkinson disease	8.681
44	Wegener granulomatosis	8.143
66	IgA nephropathy	8.050
299	Cystic fibrosis	7.965
58	Hypertrophic cardiomyopathy	7.910
85	Idiopathic interstitial pneumonia	7.906
19	Lysosomal storage disease	7.807
160	Congenital ichthyosis	7.703
45	Eosinophilic granulomatosis with Polyangiitis	6.481
283	Acquired pure red cell aplasia	6.481
286	Hereditary sideroblastic anemia	6.253
39	Toxic epidermal necrolysis	6.182
42	Polyarteritis nodosa	6.108
151	Rasmussen encephalitis	6.000
274	Osteogenesis Imperfecta	5.143
302	Leber hereditary optic neuropathy	5.000
224	Purpura nephritis	4.889
38	Stevens-Johnson syndrome	4.889
62	Paroxysmal nocturnal hemoglobinuria	4.821
326	Osteopetrosis	4.667
28	Systemic amyloidosis	4.636
63	Idiopathic thrombocytopenic purpura	4.594
90	Retinitis pigmentosa	4.424
270	Chronic recurrent multifocal osteomyelitis	4.253
113	Muscular dystrophy	4.102
43	Microscopic polyangiitis	4.010
106	Cryopyrin-associated periodic syndrome	4.000
64	Thrombotic thrombocytopenic purpura	3.637
61	Autoimmune hemolytic anemia	3.467
81	Congenital adrenal hyperplasia	3.375
37	Generalised pustular psoriasis	3.114
298	Hereditary pancreatitis	2.929
20	Adrenoleukodystrophy	2.923
35	Pemphigus	2.923
86	Pulmonary arterial hypertension	2.875
227	Osler disease	2.841
26	HTLV-1-associated myelopathy	2.737
265	Lipodystrophy	2.631
34	Neurofibromatosis	2.444
36	Epidermolysis bullosa	2.422
14	Chronic inflammatory demyelinating polyneuropathy	2.387
234	Peroxisomal disease (except Adrenoleukodystrophy)	2.387
256	Muscle glycogenosis	2.371
331	Idiopathic multicentric castleman disease	2.371
158	Tuberous sclerosis	2.217
266	Familial mediterranean fever	2.121
300	IgG4-related disease	2.014
268	Nakajo-Nishimura syndrome	2.000
325	Hereditary autoinflammatory syndrome	2.000
78	Hypopituitarism	1.972
167	Marfan syndrome	1.800
15	Inclusion body myositis	1.667
83	Addison disease	1.594
193	Prader-Willi syndrome	1.368
172	Hypophosphatasia	1.361
246	Methylmalonic acidemia	1.196
156	Rett syndrome	1.159
98	Eosinophilic gastrointestinal disease	1.067
236	Pseudohypoparathyroidism	1.067
235	Hypoparathyroidism	1.042
108	TNF receptor-associated periodic syndrome	1.000
267	Hyper-IgD syndrome	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