DR info

Clinical trials : 332 / Drugs : 234 - (DrugBank : 81) / Drug target genes : 45 - Drug target pathways : 127

Myasthenia gravis 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)
11	Myasthenia gravis
13	Multiple sclerosis/Neuromyelitis optica
46	Malignant rheumatoid arthritis
96	Crohn disease
49	Systemic lupus erythematosus
65	Primary immunodeficiency
51	Scleroderma
6	Parkinson disease
53	Sjogren syndrome
107	Juvenile idiopathic arthritis
40	Takayasu arteritis
28	Systemic amyloidosis
44	Wegener granulomatosis
283	Acquired pure red cell aplasia
60	Aplastic anemia
284	Diamond-Blackfan anemia
164	Oculocutaneous albinism
55	Relapsing polychondritis
300	IgG4-related disease
2	Amyotrophic lateral sclerosis
50	Dermatomyositis
285	Fanconi anemia
61	Autoimmune hemolytic anemia
162	Pemphigoid
41	Giant cell arteritis
62	Paroxysmal nocturnal hemoglobinuria
113	Muscular dystrophy
222	Primary nephrotic syndrome
93	Primary biliary cholangitis
85	Idiopathic interstitial pneumonia
45	Eosinophilic granulomatosis with Polyangiitis
169	Menkes disease
170	Occipital horn syndrome
256	Muscle glycogenosis
14	Chronic inflammatory demyelinating polyneuropathy
271	Ankylosing spondylitis
42	Polyarteritis nodosa
286	Hereditary sideroblastic anemia
97	Ulcerative colitis
95	Autoimmune hepatitis
226	Interstitial cystitis with Hunners ulcer
66	IgA nephropathy
19	Lysosomal storage disease
43	Microscopic polyangiitis
228	Bronchiolitis obliterans
118	Myelomeningocele
224	Purpura nephritis
269	Pyogenic arthritis
22	Moyamoya disease
234	Peroxisomal disease (except Adrenoleukodystrophy)
35	Pemphigus
70	Spinal stenosis
288	Autoimmune acquired coagulation factor deficiency
84	Sarcoidosis
26	HTLV-1-associated myelopathy
12	Congenital myasthenic syndrome
302	Leber hereditary optic neuropathy
5	Progressive supranuclear palsy
64	Thrombotic thrombocytopenic purpura
326	Osteopetrosis
58	Hypertrophic cardiomyopathy
158	Tuberous sclerosis
56	Behcet disease
57	Idiopathic dilated cardiomyopathy
151	Rasmussen encephalitis
331	Idiopathic multicentric castleman disease
38	Stevens-Johnson syndrome
20	Adrenoleukodystrophy
36	Epidermolysis bullosa
227	Osler disease
39	Toxic epidermal necrolysis
86	Pulmonary arterial hypertension
17	Multiple system atrophy
160	Congenital ichthyosis
4	Primary lateral sclerosis
90	Retinitis pigmentosa
34	Neurofibromatosis
299	Cystic fibrosis
274	Osteogenesis Imperfecta
280	Huge arteriovenous malformation with cervicofacial or limb lesion
3	Spinal muscular atrophy
323	Aromatic L-amino acid decarboxylase deficiency
206	Fragile X syndrome
127	Frontotemporal lobar degeneration
63	Idiopathic thrombocytopenic purpura
296	Biliary atresia
215	Tetralogy of Fallot
210	Single Ventricle
251	Urea cycle disorder
8	Huntington disease
78	Hypopituitarism
268	Nakajo-Nishimura syndrome
325	Hereditary autoinflammatory syndrome
337	Homocystinuria
278	Huge lymphatic malformation with cervicofacial lesion
16	Crow-Fukase syndrome
94	Primary sclerosing cholangitis
270	Chronic recurrent multifocal osteomyelitis
25	Progressive multifocal leukoencephalopathy
172	Hypophosphatasia
212	Tricuspid atresia
254	Porphyria
167	Marfan syndrome
21	Mitochondrial disease
111	Congenital myopathy
54	Adult still disease
52	Mixed connective tissue disease
220	Rapidly progressive glomerulonephritis
30	Distal myopathy