DR info

Clinical trials : 119 / Drugs : 138 - (DrugBank : 44) / Drug target genes : 59 - Drug target pathways : 111

Multiple system atrophy 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)
17	Multiple system atrophy
6	Parkinson disease
2	Amyotrophic lateral sclerosis
5	Progressive supranuclear palsy
13	Multiple sclerosis/Neuromyelitis optica
206	Fragile X syndrome
8	Huntington disease
46	Malignant rheumatoid arthritis
18	Spinocerebellar degeneration
97	Ulcerative colitis
140	Dorabe syndrome
156	Rett syndrome
3	Spinal muscular atrophy
96	Crohn disease
70	Spinal stenosis
22	Moyamoya disease
193	Prader-Willi syndrome
201	Angelman syndrome
21	Mitochondrial disease
144	Lennox-Gastaut syndrome
205	Fragile X syndrome related disease
152	PCDH19 related syndrome
296	Biliary atresia
158	Tuberous sclerosis
203	22q11.2 deletion syndrome
98	Eosinophilic gastrointestinal disease
145	West syndrome
36	Epidermolysis bullosa
272	Fibrodysplasia ossificans progressiva
4	Primary lateral sclerosis
75	Cushing disease
155	Acquired aphasia with convulsive disorder
231	Alpha-1-antitrypsin deficiency
34	Neurofibromatosis
215	Tetralogy of Fallot
113	Muscular dystrophy
84	Sarcoidosis
169	Menkes disease
170	Occipital horn syndrome
127	Frontotemporal lobar degeneration
298	Hereditary pancreatitis
118	Myelomeningocele
86	Pulmonary arterial hypertension
57	Idiopathic dilated cardiomyopathy
85	Idiopathic interstitial pneumonia
78	Hypopituitarism
7	Corticobasal degeneration
280	Huge arteriovenous malformation with cervicofacial or limb lesion
299	Cystic fibrosis
11	Myasthenia gravis
49	Systemic lupus erythematosus
278	Huge lymphatic malformation with cervicofacial lesion
288	Autoimmune acquired coagulation factor deficiency
323	Aromatic L-amino acid decarboxylase deficiency
90	Retinitis pigmentosa
167	Marfan syndrome
67	Polycystic kidney disease
226	Interstitial cystitis with Hunners ulcer
309	Progressive myoclonus epilepsy
58	Hypertrophic cardiomyopathy
210	Single Ventricle
164	Oculocutaneous albinism
66	IgA nephropathy
120	Hereditary dystonia
179	Williams syndrome
157	Sturge-Weber syndrome
74	Prolactin secreting pituitary adenoma
254	Porphyria
218	Alport syndrome
19	Lysosomal storage disease
212	Tricuspid atresia
222	Primary nephrotic syndrome
137	Focal cortical dysplasia
192	Cockayne syndrome
277	Lymphangiomatosis
281	Klippel-Trenaunay-Weber syndrome
111	Congenital myopathy
52	Mixed connective tissue disease