DR info

Clinical trials : 627 / Drugs : 443 - (DrugBank : 120) / Drug target genes : 99 - Drug target pathways : 212

Idiopathic interstitial pneumonia 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)
85	Idiopathic interstitial pneumonia
51	Scleroderma
46	Malignant rheumatoid arthritis
13	Multiple sclerosis/Neuromyelitis optica
2	Amyotrophic lateral sclerosis
65	Primary immunodeficiency
228	Bronchiolitis obliterans
28	Systemic amyloidosis
6	Parkinson disease
34	Neurofibromatosis
331	Idiopathic multicentric castleman disease
26	HTLV-1-associated myelopathy
42	Polyarteritis nodosa
49	Systemic lupus erythematosus
96	Crohn disease
222	Primary nephrotic syndrome
89	Lymphangioleiomyomatosis
86	Pulmonary arterial hypertension
227	Osler disease
113	Muscular dystrophy
164	Oculocutaneous albinism
56	Behcet disease
127	Frontotemporal lobar degeneration
210	Single Ventricle
45	Eosinophilic granulomatosis with Polyangiitis
41	Giant cell arteritis
97	Ulcerative colitis
93	Primary biliary cholangitis
285	Fanconi anemia
58	Hypertrophic cardiomyopathy
60	Aplastic anemia
11	Myasthenia gravis
266	Familial mediterranean fever
66	IgA nephropathy
283	Acquired pure red cell aplasia
215	Tetralogy of Fallot
284	Diamond-Blackfan anemia
50	Dermatomyositis
39	Toxic epidermal necrolysis
5	Progressive supranuclear palsy
19	Lysosomal storage disease
162	Pemphigoid
38	Stevens-Johnson syndrome
224	Purpura nephritis
102	Rubinstein-Taybi syndrome
36	Epidermolysis bullosa
3	Spinal muscular atrophy
40	Takayasu arteritis
61	Autoimmune hemolytic anemia
8	Huntington disease
62	Paroxysmal nocturnal hemoglobinuria
90	Retinitis pigmentosa
20	Adrenoleukodystrophy
35	Pemphigus
274	Osteogenesis Imperfecta
151	Rasmussen encephalitis
226	Interstitial cystitis with Hunners ulcer
84	Sarcoidosis
57	Idiopathic dilated cardiomyopathy
234	Peroxisomal disease (except Adrenoleukodystrophy)
326	Osteopetrosis
88	Chronic thromboembolic pulmonary hypertension
70	Spinal stenosis
53	Sjogren syndrome
302	Leber hereditary optic neuropathy
211	Hypoplastic left heart syndrome
43	Microscopic polyangiitis
17	Multiple system atrophy
95	Autoimmune hepatitis
256	Muscle glycogenosis
233	Wolfram syndrome
286	Hereditary sideroblastic anemia
269	Pyogenic arthritis
107	Juvenile idiopathic arthritis
78	Hypopituitarism
64	Thrombotic thrombocytopenic purpura
55	Relapsing polychondritis
63	Idiopathic thrombocytopenic purpura
299	Cystic fibrosis
67	Polycystic kidney disease
87	Pulmonary veno-occlusive disease
280	Huge arteriovenous malformation with cervicofacial or limb lesion
18	Spinocerebellar degeneration
158	Tuberous sclerosis
278	Huge lymphatic malformation with cervicofacial lesion
160	Congenital ichthyosis
169	Menkes disease
170	Occipital horn syndrome
47	Buerger disease
44	Wegener granulomatosis
98	Eosinophilic gastrointestinal disease
21	Mitochondrial disease
91	Budd-Chiari syndrome
71	Idiopathic osteonecrosis of the femoral head
298	Hereditary pancreatitis
206	Fragile X syndrome
94	Primary sclerosing cholangitis
271	Ankylosing spondylitis
118	Myelomeningocele
282	Congenital dyserythropoietic anemia
203	22q11.2 deletion syndrome
301	Macular dystrophy
157	Sturge-Weber syndrome
276	Achondroplasia
16	Crow-Fukase syndrome
166	Pseudoxanthoma elasticum
294	Congenital diaphragmatic hernia
300	IgG4-related disease
205	Fragile X syndrome related disease
288	Autoimmune acquired coagulation factor deficiency
218	Alport syndrome
83	Addison disease
4	Primary lateral sclerosis
14	Chronic inflammatory demyelinating polyneuropathy
25	Progressive multifocal leukoencephalopathy
212	Tricuspid atresia
22	Moyamoya disease
156	Rett syndrome
149	Hemiconvulsion hemiplegia epilepsy syndrome
106	Cryopyrin-associated periodic syndrome
238	Vitamin D-resistant rickets
235	Hypoparathyroidism
137	Focal cortical dysplasia
192	Cockayne syndrome
277	Lymphangiomatosis
281	Klippel-Trenaunay-Weber syndrome
111	Congenital myopathy
108	TNF receptor-associated periodic syndrome
267	Hyper-IgD syndrome
52	Mixed connective tissue disease
220	Rapidly progressive glomerulonephritis
30	Distal myopathy