DR info

Clinical trials : 646 / Drugs : 471 - (DrugBank : 105) / Drug target genes : 59 - Drug target pathways : 170

Muscular dystrophy 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)
113	Muscular dystrophy
46	Malignant rheumatoid arthritis
13	Multiple sclerosis/Neuromyelitis optica
96	Crohn disease
6	Parkinson disease
2	Amyotrophic lateral sclerosis
97	Ulcerative colitis
8	Huntington disease
85	Idiopathic interstitial pneumonia
107	Juvenile idiopathic arthritis
49	Systemic lupus erythematosus
86	Pulmonary arterial hypertension
70	Spinal stenosis
226	Interstitial cystitis with Hunners ulcer
58	Hypertrophic cardiomyopathy
65	Primary immunodeficiency
299	Cystic fibrosis
17	Multiple system atrophy
222	Primary nephrotic syndrome
38	Stevens-Johnson syndrome
127	Frontotemporal lobar degeneration
51	Scleroderma
11	Myasthenia gravis
28	Systemic amyloidosis
215	Tetralogy of Fallot
206	Fragile X syndrome
78	Hypopituitarism
5	Progressive supranuclear palsy
21	Mitochondrial disease
34	Neurofibromatosis
168	Ehlers-Danlos syndrome
57	Idiopathic dilated cardiomyopathy
169	Menkes disease
170	Occipital horn syndrome
53	Sjogren syndrome
36	Epidermolysis bullosa
118	Myelomeningocele
224	Purpura nephritis
66	IgA nephropathy
158	Tuberous sclerosis
285	Fanconi anemia
60	Aplastic anemia
1	Spinal and bulbar muscular atrophy
302	Leber hereditary optic neuropathy
22	Moyamoya disease
3	Spinal muscular atrophy
64	Thrombotic thrombocytopenic purpura
227	Osler disease
210	Single Ventricle
151	Rasmussen encephalitis
83	Addison disease
41	Giant cell arteritis
164	Oculocutaneous albinism
19	Lysosomal storage disease
50	Dermatomyositis
4	Primary lateral sclerosis
274	Osteogenesis Imperfecta
298	Hereditary pancreatitis
84	Sarcoidosis
269	Pyogenic arthritis
256	Muscle glycogenosis
39	Toxic epidermal necrolysis
18	Spinocerebellar degeneration
63	Idiopathic thrombocytopenic purpura
228	Bronchiolitis obliterans
90	Retinitis pigmentosa
156	Rett syndrome
193	Prader-Willi syndrome
81	Congenital adrenal hyperplasia
286	Hereditary sideroblastic anemia
45	Eosinophilic granulomatosis with Polyangiitis
288	Autoimmune acquired coagulation factor deficiency
283	Acquired pure red cell aplasia
67	Polycystic kidney disease
95	Autoimmune hepatitis
171	Wilson disease
323	Aromatic L-amino acid decarboxylase deficiency
225	Congenital nephrogenic diabetes insipidus
280	Huge arteriovenous malformation with cervicofacial or limb lesion
62	Paroxysmal nocturnal hemoglobinuria
284	Diamond-Blackfan anemia
218	Alport syndrome
76	Pituitary gonadotropin secretion hyperthyroidism
93	Primary biliary cholangitis
231	Alpha-1-antitrypsin deficiency
326	Osteopetrosis
56	Behcet disease
40	Takayasu arteritis
205	Fragile X syndrome related disease
10	Charcot-Marie-Tooth disease
42	Polyarteritis nodosa
75	Cushing disease
271	Ankylosing spondylitis
160	Congenital ichthyosis
55	Relapsing polychondritis
234	Peroxisomal disease (except Adrenoleukodystrophy)
251	Urea cycle disorder
333	Hutchinson-Gilford syndrome
71	Idiopathic osteonecrosis of the femoral head
162	Pemphigoid
212	Tricuspid atresia
20	Adrenoleukodystrophy
203	22q11.2 deletion syndrome
77	Growth hormone secreting pituitary adenoma
337	Homocystinuria
257	Hepatic glycogenosis
282	Congenital dyserythropoietic anemia
26	HTLV-1-associated myelopathy
61	Autoimmune hemolytic anemia
294	Congenital diaphragmatic hernia
211	Hypoplastic left heart syndrome
278	Huge lymphatic malformation with cervicofacial lesion
167	Marfan syndrome
114	Non-dystrophic myotonia syndrome
265	Lipodystrophy
74	Prolactin secreting pituitary adenoma
301	Macular dystrophy
179	Williams syndrome
238	Vitamin D-resistant rickets
235	Hypoparathyroidism
111	Congenital myopathy
108	TNF receptor-associated periodic syndrome
267	Hyper-IgD syndrome
191	Werner syndrome
220	Rapidly progressive glomerulonephritis
30	Distal myopathy