DR info

Clinical trials : 90 / Drugs : 122 - (DrugBank : 47) / Drug target genes : 34 - Drug target pathways : 144

Pemphigoid and other diseases between which drug repositioning (DR) might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Score (Drug repositionability)

ID	Diseases (Sorted by score)	Score
162	Pemphigoid	-
46	Malignant rheumatoid arthritis	26.036
96	Crohn disease	18.390
13	Multiple sclerosis/Neuromyelitis optica	18.045
50	Dermatomyositis	16.705
53	Sjogren syndrome	16.279
51	Scleroderma	16.094
97	Ulcerative colitis	15.795
56	Behcet disease	15.194
49	Systemic lupus erythematosus	14.770
269	Pyogenic arthritis	13.463
271	Ankylosing spondylitis	13.410
41	Giant cell arteritis	13.004
93	Primary biliary cholangitis	12.761
107	Juvenile idiopathic arthritis	12.650
65	Primary immunodeficiency	12.641
45	Eosinophilic granulomatosis with Polyangiitis	12.209
40	Takayasu arteritis	11.727
84	Sarcoidosis	11.614
11	Myasthenia gravis	9.545
160	Congenital ichthyosis	9.455
66	IgA nephropathy	9.164
60	Aplastic anemia	8.626
284	Diamond-Blackfan anemia	8.529
2	Amyotrophic lateral sclerosis	8.524
6	Parkinson disease	8.459
228	Bronchiolitis obliterans	8.225
283	Acquired pure red cell aplasia	8.148
42	Polyarteritis nodosa	7.888
226	Interstitial cystitis with Hunners ulcer	7.703
224	Purpura nephritis	7.677
44	Wegener granulomatosis	7.508
62	Paroxysmal nocturnal hemoglobinuria	7.508
285	Fanconi anemia	7.418
55	Relapsing polychondritis	7.364
299	Cystic fibrosis	7.115
85	Idiopathic interstitial pneumonia	7.079
164	Oculocutaneous albinism	7.059
222	Primary nephrotic syndrome	6.800
28	Systemic amyloidosis	6.673
19	Lysosomal storage disease	6.606
63	Idiopathic thrombocytopenic purpura	6.400
286	Hereditary sideroblastic anemia	6.311
35	Pemphigus	6.198
151	Rasmussen encephalitis	6.000
61	Autoimmune hemolytic anemia	5.818
95	Autoimmune hepatitis	5.555
43	Microscopic polyangiitis	5.403
20	Adrenoleukodystrophy	5.132
302	Leber hereditary optic neuropathy	5.000
39	Toxic epidermal necrolysis	4.994
326	Osteopetrosis	4.970
234	Peroxisomal disease (except Adrenoleukodystrophy)	4.702
36	Epidermolysis bullosa	4.453
38	Stevens-Johnson syndrome	4.059
64	Thrombotic thrombocytopenic purpura	3.898
26	HTLV-1-associated myelopathy	3.215
274	Osteogenesis Imperfecta	3.195
227	Osler disease	3.163
300	IgG4-related disease	3.055
265	Lipodystrophy	2.970
270	Chronic recurrent multifocal osteomyelitis	2.828
94	Primary sclerosing cholangitis	2.641
158	Tuberous sclerosis	2.588
37	Generalised pustular psoriasis	2.564
34	Neurofibromatosis	2.497
98	Eosinophilic gastrointestinal disease	2.426
87	Pulmonary veno-occlusive disease	2.318
58	Hypertrophic cardiomyopathy	2.289
113	Muscular dystrophy	2.139
268	Nakajo-Nishimura syndrome	2.000
325	Hereditary autoinflammatory syndrome	2.000
8	Huntington disease	1.944
90	Retinitis pigmentosa	1.692
88	Chronic thromboembolic pulmonary hypertension	1.566
256	Muscle glycogenosis	1.442
331	Idiopathic multicentric castleman disease	1.442
86	Pulmonary arterial hypertension	1.385
172	Hypophosphatasia	1.374
246	Methylmalonic acidemia	1.312
78	Hypopituitarism	1.240
236	Pseudohypoparathyroidism	1.188
235	Hypoparathyroidism	1.061
89	Lymphangioleiomyomatosis	1.006
52	Mixed connective tissue disease	1.000
220	Rapidly progressive glomerulonephritis	1.000
30	Distal myopathy	1.000