DR info

Clinical trials : 2,630 / Drugs : 1,459 - (DrugBank : 265) / Drug target genes : 144 - Drug target pathways : 202

Ulcerative colitis 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)
97	Ulcerative colitis
96	Crohn disease
13	Multiple sclerosis/Neuromyelitis optica
46	Malignant rheumatoid arthritis
6	Parkinson disease
2	Amyotrophic lateral sclerosis
8	Huntington disease
156	Rett syndrome
140	Dorabe syndrome
144	Lennox-Gastaut syndrome
21	Mitochondrial disease
84	Sarcoidosis
49	Systemic lupus erythematosus
206	Fragile X syndrome
107	Juvenile idiopathic arthritis
298	Hereditary pancreatitis
193	Prader-Willi syndrome
18	Spinocerebellar degeneration
50	Dermatomyositis
70	Spinal stenosis
231	Alpha-1-antitrypsin deficiency
17	Multiple system atrophy
271	Ankylosing spondylitis
158	Tuberous sclerosis
36	Epidermolysis bullosa
3	Spinal muscular atrophy
51	Scleroderma
226	Interstitial cystitis with Hunners ulcer
5	Progressive supranuclear palsy
41	Giant cell arteritis
98	Eosinophilic gastrointestinal disease
299	Cystic fibrosis
65	Primary immunodeficiency
205	Fragile X syndrome related disease
145	West syndrome
53	Sjogren syndrome
56	Behcet disease
34	Neurofibromatosis
113	Muscular dystrophy
272	Fibrodysplasia ossificans progressiva
152	PCDH19 related syndrome
162	Pemphigoid
201	Angelman syndrome
40	Takayasu arteritis
78	Hypopituitarism
86	Pulmonary arterial hypertension
203	22q11.2 deletion syndrome
265	Lipodystrophy
60	Aplastic anemia
58	Hypertrophic cardiomyopathy
75	Cushing disease
93	Primary biliary cholangitis
22	Moyamoya disease
155	Acquired aphasia with convulsive disorder
269	Pyogenic arthritis
85	Idiopathic interstitial pneumonia
296	Biliary atresia
63	Idiopathic thrombocytopenic purpura
66	IgA nephropathy
55	Relapsing polychondritis
222	Primary nephrotic syndrome
38	Stevens-Johnson syndrome
45	Eosinophilic granulomatosis with Polyangiitis
160	Congenital ichthyosis
284	Diamond-Blackfan anemia
285	Fanconi anemia
44	Wegener granulomatosis
164	Oculocutaneous albinism
224	Purpura nephritis
95	Autoimmune hepatitis
11	Myasthenia gravis
37	Generalised pustular psoriasis
127	Frontotemporal lobar degeneration
28	Systemic amyloidosis
90	Retinitis pigmentosa
42	Polyarteritis nodosa
256	Muscle glycogenosis
19	Lysosomal storage disease
283	Acquired pure red cell aplasia
286	Hereditary sideroblastic anemia
151	Rasmussen encephalitis
10	Charcot-Marie-Tooth disease
81	Congenital adrenal hyperplasia
236	Pseudohypoparathyroidism
302	Leber hereditary optic neuropathy
294	Congenital diaphragmatic hernia
20	Adrenoleukodystrophy
35	Pemphigus
43	Microscopic polyangiitis
39	Toxic epidermal necrolysis
228	Bronchiolitis obliterans
326	Osteopetrosis
62	Paroxysmal nocturnal hemoglobinuria
168	Ehlers-Danlos syndrome
246	Methylmalonic acidemia
225	Congenital nephrogenic diabetes insipidus
67	Polycystic kidney disease
167	Marfan syndrome
94	Primary sclerosing cholangitis
25	Progressive multifocal leukoencephalopathy
300	IgG4-related disease
15	Inclusion body myositis
64	Thrombotic thrombocytopenic purpura
26	HTLV-1-associated myelopathy
234	Peroxisomal disease (except Adrenoleukodystrophy)
171	Wilson disease
310	Congenital anomalies syndrome
229	Autoimmune pulmonary alveolar proteinosis
114	Non-dystrophic myotonia syndrome
215	Tetralogy of Fallot
179	Williams syndrome
4	Primary lateral sclerosis
274	Osteogenesis Imperfecta
218	Alport syndrome
1	Spinal and bulbar muscular atrophy
251	Urea cycle disorder
91	Budd-Chiari syndrome
202	Smith-Magenis syndrome
61	Autoimmune hemolytic anemia
77	Growth hormone secreting pituitary adenoma
268	Nakajo-Nishimura syndrome
325	Hereditary autoinflammatory syndrome
337	Homocystinuria
263	Cerebrotendinous xanthomatosis
257	Hepatic glycogenosis
282	Congenital dyserythropoietic anemia
120	Hereditary dystonia
227	Osler disease
149	Hemiconvulsion hemiplegia epilepsy syndrome
270	Chronic recurrent multifocal osteomyelitis
288	Autoimmune acquired coagulation factor deficiency
172	Hypophosphatasia
88	Chronic thromboembolic pulmonary hypertension
280	Huge arteriovenous malformation with cervicofacial or limb lesion
301	Macular dystrophy
57	Idiopathic dilated cardiomyopathy
79	Homozygous familial hypercholesterolemia
106	Cryopyrin-associated periodic syndrome
235	Hypoparathyroidism
71	Idiopathic osteonecrosis of the femoral head
317	Trifunctional protein deficiency
52	Mixed connective tissue disease
220	Rapidly progressive glomerulonephritis
30	Distal myopathy