DR info

Clinical trials : 145 / Drugs : 156 - (DrugBank : 51) / Drug target genes : 64 - Drug target pathways : 146

Interstitial cystitis with Hunners ulcer 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)
226	Interstitial cystitis with Hunners ulcer
13	Multiple sclerosis/Neuromyelitis optica
6	Parkinson disease
96	Crohn disease
46	Malignant rheumatoid arthritis
299	Cystic fibrosis
2	Amyotrophic lateral sclerosis
97	Ulcerative colitis
51	Scleroderma
63	Idiopathic thrombocytopenic purpura
246	Methylmalonic acidemia
70	Spinal stenosis
53	Sjogren syndrome
107	Juvenile idiopathic arthritis
236	Pseudohypoparathyroidism
113	Muscular dystrophy
86	Pulmonary arterial hypertension
298	Hereditary pancreatitis
78	Hypopituitarism
38	Stevens-Johnson syndrome
58	Hypertrophic cardiomyopathy
50	Dermatomyositis
45	Eosinophilic granulomatosis with Polyangiitis
224	Purpura nephritis
156	Rett syndrome
36	Epidermolysis bullosa
162	Pemphigoid
11	Myasthenia gravis
21	Mitochondrial disease
95	Autoimmune hepatitis
28	Systemic amyloidosis
65	Primary immunodeficiency
42	Polyarteritis nodosa
49	Systemic lupus erythematosus
84	Sarcoidosis
8	Huntington disease
90	Retinitis pigmentosa
10	Charcot-Marie-Tooth disease
193	Prader-Willi syndrome
19	Lysosomal storage disease
151	Rasmussen encephalitis
85	Idiopathic interstitial pneumonia
26	HTLV-1-associated myelopathy
227	Osler disease
271	Ankylosing spondylitis
302	Leber hereditary optic neuropathy
40	Takayasu arteritis
158	Tuberous sclerosis
39	Toxic epidermal necrolysis
5	Progressive supranuclear palsy
140	Dorabe syndrome
56	Behcet disease
144	Lennox-Gastaut syndrome
284	Diamond-Blackfan anemia
234	Peroxisomal disease (except Adrenoleukodystrophy)
285	Fanconi anemia
60	Aplastic anemia
168	Ehlers-Danlos syndrome
41	Giant cell arteritis
283	Acquired pure red cell aplasia
231	Alpha-1-antitrypsin deficiency
66	IgA nephropathy
254	Porphyria
265	Lipodystrophy
43	Microscopic polyangiitis
167	Marfan syndrome
269	Pyogenic arthritis
62	Paroxysmal nocturnal hemoglobinuria
34	Neurofibromatosis
20	Adrenoleukodystrophy
222	Primary nephrotic syndrome
64	Thrombotic thrombocytopenic purpura
228	Bronchiolitis obliterans
164	Oculocutaneous albinism
55	Relapsing polychondritis
286	Hereditary sideroblastic anemia
61	Autoimmune hemolytic anemia
206	Fragile X syndrome
127	Frontotemporal lobar degeneration
323	Aromatic L-amino acid decarboxylase deficiency
98	Eosinophilic gastrointestinal disease
169	Menkes disease
170	Occipital horn syndrome
280	Huge arteriovenous malformation with cervicofacial or limb lesion
296	Biliary atresia
300	IgG4-related disease
1	Spinal and bulbar muscular atrophy
93	Primary biliary cholangitis
17	Multiple system atrophy
215	Tetralogy of Fallot
160	Congenital ichthyosis
22	Moyamoya disease
81	Congenital adrenal hyperplasia
251	Urea cycle disorder
256	Muscle glycogenosis
118	Myelomeningocele
212	Tricuspid atresia
44	Wegener granulomatosis
35	Pemphigus
274	Osteogenesis Imperfecta
337	Homocystinuria
120	Hereditary dystonia
294	Congenital diaphragmatic hernia
157	Sturge-Weber syndrome
278	Huge lymphatic malformation with cervicofacial lesion
326	Osteopetrosis
114	Non-dystrophic myotonia syndrome
288	Autoimmune acquired coagulation factor deficiency
83	Addison disease
124	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
171	Wilson disease
149	Hemiconvulsion hemiplegia epilepsy syndrome
94	Primary sclerosing cholangitis
317	Trifunctional protein deficiency
220	Rapidly progressive glomerulonephritis
30	Distal myopathy