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

ID	Diseases (Sorted by score)	Score
256	Muscle glycogenosis	-
13	Multiple sclerosis/Neuromyelitis optica	17.578
46	Malignant rheumatoid arthritis	14.995
6	Parkinson disease	14.982
34	Neurofibromatosis	12.013
65	Primary immunodeficiency	11.961
51	Scleroderma	11.654
96	Crohn disease	11.260
127	Frontotemporal lobar degeneration	10.161
2	Amyotrophic lateral sclerosis	10.081
11	Myasthenia gravis	8.711
331	Idiopathic multicentric castleman disease	8.617
86	Pulmonary arterial hypertension	7.397
107	Juvenile idiopathic arthritis	7.339
49	Systemic lupus erythematosus	7.265
97	Ulcerative colitis	7.074
222	Primary nephrotic syndrome	7.060
102	Rubinstein-Taybi syndrome	7.000
89	Lymphangioleiomyomatosis	6.795
84	Sarcoidosis	6.648
53	Sjogren syndrome	6.250
3	Spinal muscular atrophy	5.376
5	Progressive supranuclear palsy	5.104
233	Wolfram syndrome	5.029
271	Ankylosing spondylitis	4.878
85	Idiopathic interstitial pneumonia	4.692
58	Hypertrophic cardiomyopathy	4.637
35	Pemphigus	4.223
26	HTLV-1-associated myelopathy	4.126
1	Spinal and bulbar muscular atrophy	4.065
113	Muscular dystrophy	3.587
28	Systemic amyloidosis	3.484
70	Spinal stenosis	3.484
231	Alpha-1-antitrypsin deficiency	3.421
44	Wegener granulomatosis	3.387
168	Ehlers-Danlos syndrome	3.136
40	Takayasu arteritis	3.098
38	Stevens-Johnson syndrome	3.097
36	Epidermolysis bullosa	3.034
298	Hereditary pancreatitis	2.960
283	Acquired pure red cell aplasia	2.774
10	Charcot-Marie-Tooth disease	2.713
50	Dermatomyositis	2.371
90	Retinitis pigmentosa	2.355
226	Interstitial cystitis with Hunners ulcer	2.173
19	Lysosomal storage disease	2.130
41	Giant cell arteritis	2.041
149	Hemiconvulsion hemiplegia epilepsy syndrome	2.040
8	Huntington disease	2.032
268	Nakajo-Nishimura syndrome	2.000
325	Hereditary autoinflammatory syndrome	2.000
337	Homocystinuria	2.000
114	Non-dystrophic myotonia syndrome	1.971
60	Aplastic anemia	1.853
193	Prader-Willi syndrome	1.731
156	Rett syndrome	1.538
285	Fanconi anemia	1.505
300	IgG4-related disease	1.445
162	Pemphigoid	1.442
228	Bronchiolitis obliterans	1.442
93	Primary biliary cholangitis	1.406
158	Tuberous sclerosis	1.406
172	Hypophosphatasia	1.376
45	Eosinophilic granulomatosis with Polyangiitis	1.290
215	Tetralogy of Fallot	1.290
140	Dorabe syndrome	1.243
144	Lennox-Gastaut syndrome	1.234
62	Paroxysmal nocturnal hemoglobinuria	1.180
284	Diamond-Blackfan anemia	1.150
61	Autoimmune hemolytic anemia	1.074
251	Urea cycle disorder	1.065
42	Polyarteritis nodosa	1.052
299	Cystic fibrosis	1.025
277	Lymphangiomatosis	1.000
281	Klippel-Trenaunay-Weber syndrome	1.000
111	Congenital myopathy	1.000
52	Mixed connective tissue disease	1.000
137	Focal cortical dysplasia	1.000
192	Cockayne syndrome	1.000