DR info

Clinical trials : 180 / Drugs : 133 - (DrugBank : 29) / Drug target genes : 25 - Drug target pathways : 105

Muscle glycogenosis 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)
256	Muscle glycogenosis
13	Multiple sclerosis/Neuromyelitis optica
46	Malignant rheumatoid arthritis
6	Parkinson disease
34	Neurofibromatosis
65	Primary immunodeficiency
51	Scleroderma
96	Crohn disease
127	Frontotemporal lobar degeneration
2	Amyotrophic lateral sclerosis
11	Myasthenia gravis
331	Idiopathic multicentric castleman disease
86	Pulmonary arterial hypertension
107	Juvenile idiopathic arthritis
49	Systemic lupus erythematosus
97	Ulcerative colitis
222	Primary nephrotic syndrome
102	Rubinstein-Taybi syndrome
89	Lymphangioleiomyomatosis
84	Sarcoidosis
53	Sjogren syndrome
3	Spinal muscular atrophy
5	Progressive supranuclear palsy
233	Wolfram syndrome
271	Ankylosing spondylitis
85	Idiopathic interstitial pneumonia
58	Hypertrophic cardiomyopathy
35	Pemphigus
26	HTLV-1-associated myelopathy
1	Spinal and bulbar muscular atrophy
113	Muscular dystrophy
28	Systemic amyloidosis
70	Spinal stenosis
231	Alpha-1-antitrypsin deficiency
44	Wegener granulomatosis
168	Ehlers-Danlos syndrome
40	Takayasu arteritis
38	Stevens-Johnson syndrome
36	Epidermolysis bullosa
298	Hereditary pancreatitis
283	Acquired pure red cell aplasia
10	Charcot-Marie-Tooth disease
50	Dermatomyositis
90	Retinitis pigmentosa
226	Interstitial cystitis with Hunners ulcer
19	Lysosomal storage disease
41	Giant cell arteritis
149	Hemiconvulsion hemiplegia epilepsy syndrome
8	Huntington disease
268	Nakajo-Nishimura syndrome
325	Hereditary autoinflammatory syndrome
337	Homocystinuria
114	Non-dystrophic myotonia syndrome
60	Aplastic anemia
193	Prader-Willi syndrome
156	Rett syndrome
285	Fanconi anemia
300	IgG4-related disease
162	Pemphigoid
228	Bronchiolitis obliterans
93	Primary biliary cholangitis
158	Tuberous sclerosis
172	Hypophosphatasia
45	Eosinophilic granulomatosis with Polyangiitis
215	Tetralogy of Fallot
140	Dorabe syndrome
144	Lennox-Gastaut syndrome
62	Paroxysmal nocturnal hemoglobinuria
284	Diamond-Blackfan anemia
61	Autoimmune hemolytic anemia
251	Urea cycle disorder
42	Polyarteritis nodosa
299	Cystic fibrosis
277	Lymphangiomatosis
281	Klippel-Trenaunay-Weber syndrome
111	Congenital myopathy
52	Mixed connective tissue disease
137	Focal cortical dysplasia
192	Cockayne syndrome