DR info

Clinical trials : 163 / Drugs : 185 - (DrugBank : 46) / Drug target genes : 50 - Drug target pathways : 125

Epidermolysis bullosa 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)
36	Epidermolysis bullosa
13	Multiple sclerosis/Neuromyelitis optica
46	Malignant rheumatoid arthritis
96	Crohn disease
6	Parkinson disease
2	Amyotrophic lateral sclerosis
97	Ulcerative colitis
298	Hereditary pancreatitis
158	Tuberous sclerosis
231	Alpha-1-antitrypsin deficiency
70	Spinal stenosis
84	Sarcoidosis
193	Prader-Willi syndrome
140	Dorabe syndrome
144	Lennox-Gastaut syndrome
152	PCDH19 related syndrome
34	Neurofibromatosis
156	Rett syndrome
145	West syndrome
8	Huntington disease
201	Angelman syndrome
98	Eosinophilic gastrointestinal disease
205	Fragile X syndrome related disease
17	Multiple system atrophy
75	Cushing disease
272	Fibrodysplasia ossificans progressiva
22	Moyamoya disease
51	Scleroderma
155	Acquired aphasia with convulsive disorder
296	Biliary atresia
18	Spinocerebellar degeneration
206	Fragile X syndrome
38	Stevens-Johnson syndrome
53	Sjogren syndrome
21	Mitochondrial disease
5	Progressive supranuclear palsy
19	Lysosomal storage disease
3	Spinal muscular atrophy
62	Paroxysmal nocturnal hemoglobinuria
226	Interstitial cystitis with Hunners ulcer
283	Acquired pure red cell aplasia
85	Idiopathic interstitial pneumonia
28	Systemic amyloidosis
45	Eosinophilic granulomatosis with Polyangiitis
113	Muscular dystrophy
39	Toxic epidermal necrolysis
49	Systemic lupus erythematosus
234	Peroxisomal disease (except Adrenoleukodystrophy)
284	Diamond-Blackfan anemia
285	Fanconi anemia
60	Aplastic anemia
61	Autoimmune hemolytic anemia
66	IgA nephropathy
95	Autoimmune hepatitis
42	Polyarteritis nodosa
107	Juvenile idiopathic arthritis
302	Leber hereditary optic neuropathy
224	Purpura nephritis
65	Primary immunodeficiency
286	Hereditary sideroblastic anemia
20	Adrenoleukodystrophy
162	Pemphigoid
228	Bronchiolitis obliterans
41	Giant cell arteritis
58	Hypertrophic cardiomyopathy
164	Oculocutaneous albinism
160	Congenital ichthyosis
151	Rasmussen encephalitis
168	Ehlers-Danlos syndrome
11	Myasthenia gravis
326	Osteopetrosis
10	Charcot-Marie-Tooth disease
40	Takayasu arteritis
55	Relapsing polychondritis
222	Primary nephrotic syndrome
63	Idiopathic thrombocytopenic purpura
256	Muscle glycogenosis
274	Osteogenesis Imperfecta
299	Cystic fibrosis
269	Pyogenic arthritis
86	Pulmonary arterial hypertension
93	Primary biliary cholangitis
1	Spinal and bulbar muscular atrophy
64	Thrombotic thrombocytopenic purpura
50	Dermatomyositis
94	Primary sclerosing cholangitis
56	Behcet disease
227	Osler disease
26	HTLV-1-associated myelopathy
127	Frontotemporal lobar degeneration
157	Sturge-Weber syndrome
90	Retinitis pigmentosa
114	Non-dystrophic myotonia syndrome
35	Pemphigus
271	Ankylosing spondylitis
43	Microscopic polyangiitis
37	Generalised pustular psoriasis
44	Wegener granulomatosis
137	Focal cortical dysplasia
192	Cockayne syndrome
277	Lymphangiomatosis
281	Klippel-Trenaunay-Weber syndrome
52	Mixed connective tissue disease