53. Sjogren syndrome Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 305 / Drugs : 325 - (DrugBank : 104) / Drug target genes : 58 - Drug target pathways : 188
Sjogren syndrome 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) |
---|---|
53 | Sjogren syndrome |
46 | Malignant rheumatoid arthritis |
13 | Multiple sclerosis/Neuromyelitis optica |
49 | Systemic lupus erythematosus |
96 | Crohn disease |
65 | Primary immunodeficiency |
51 | Scleroderma |
97 | Ulcerative colitis |
107 | Juvenile idiopathic arthritis |
162 | Pemphigoid |
41 | Giant cell arteritis |
50 | Dermatomyositis |
11 | Myasthenia gravis |
40 | Takayasu arteritis |
226 | Interstitial cystitis with Hunners ulcer |
271 | Ankylosing spondylitis |
84 | Sarcoidosis |
2 | Amyotrophic lateral sclerosis |
60 | Aplastic anemia |
285 | Fanconi anemia |
93 | Primary biliary cholangitis |
55 | Relapsing polychondritis |
160 | Congenital ichthyosis |
38 | Stevens-Johnson syndrome |
269 | Pyogenic arthritis |
19 | Lysosomal storage disease |
44 | Wegener granulomatosis |
284 | Diamond-Blackfan anemia |
95 | Autoimmune hepatitis |
56 | Behcet disease |
36 | Epidermolysis bullosa |
39 | Toxic epidermal necrolysis |
45 | Eosinophilic granulomatosis with Polyangiitis |
26 | HTLV-1-associated myelopathy |
28 | Systemic amyloidosis |
42 | Polyarteritis nodosa |
62 | Paroxysmal nocturnal hemoglobinuria |
6 | Parkinson disease |
283 | Acquired pure red cell aplasia |
299 | Cystic fibrosis |
300 | IgG4-related disease |
61 | Autoimmune hemolytic anemia |
228 | Bronchiolitis obliterans |
164 | Oculocutaneous albinism |
113 | Muscular dystrophy |
222 | Primary nephrotic syndrome |
86 | Pulmonary arterial hypertension |
43 | Microscopic polyangiitis |
256 | Muscle glycogenosis |
286 | Hereditary sideroblastic anemia |
151 | Rasmussen encephalitis |
224 | Purpura nephritis |
66 | IgA nephropathy |
64 | Thrombotic thrombocytopenic purpura |
35 | Pemphigus |
63 | Idiopathic thrombocytopenic purpura |
85 | Idiopathic interstitial pneumonia |
302 | Leber hereditary optic neuropathy |
37 | Generalised pustular psoriasis |
326 | Osteopetrosis |
20 | Adrenoleukodystrophy |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
227 | Osler disease |
270 | Chronic recurrent multifocal osteomyelitis |
83 | Addison disease |
58 | Hypertrophic cardiomyopathy |
1 | Spinal and bulbar muscular atrophy |
94 | Primary sclerosing cholangitis |
98 | Eosinophilic gastrointestinal disease |
168 | Ehlers-Danlos syndrome |
296 | Biliary atresia |
274 | Osteogenesis Imperfecta |
156 | Rett syndrome |
90 | Retinitis pigmentosa |
298 | Hereditary pancreatitis |
10 | Charcot-Marie-Tooth disease |
331 | Idiopathic multicentric castleman disease |
34 | Neurofibromatosis |
231 | Alpha-1-antitrypsin deficiency |
158 | Tuberous sclerosis |
268 | Nakajo-Nishimura syndrome |
325 | Hereditary autoinflammatory syndrome |
127 | Frontotemporal lobar degeneration |
159 | Xeroderma pigmentosum |
114 | Non-dystrophic myotonia syndrome |
254 | Porphyria |
76 | Pituitary gonadotropin secretion hyperthyroidism |
70 | Spinal stenosis |
25 | Progressive multifocal leukoencephalopathy |
172 | Hypophosphatasia |
5 | Progressive supranuclear palsy |
235 | Hypoparathyroidism |
54 | Adult still disease |
52 | Mixed connective tissue disease |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |