41. Giant cell arteritis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 131 / Drugs : 139 - (DrugBank : 36) / Drug target genes : 33 - Drug target pathways : 125
Giant cell arteritis 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) |
---|---|
41 | Giant cell arteritis |
46 | Malignant rheumatoid arthritis |
13 | Multiple sclerosis/Neuromyelitis optica |
50 | Dermatomyositis |
97 | Ulcerative colitis |
51 | Scleroderma |
96 | Crohn disease |
49 | Systemic lupus erythematosus |
40 | Takayasu arteritis |
65 | Primary immunodeficiency |
53 | Sjogren syndrome |
107 | Juvenile idiopathic arthritis |
84 | Sarcoidosis |
56 | Behcet disease |
269 | Pyogenic arthritis |
162 | Pemphigoid |
93 | Primary biliary cholangitis |
45 | Eosinophilic granulomatosis with Polyangiitis |
271 | Ankylosing spondylitis |
55 | Relapsing polychondritis |
42 | Polyarteritis nodosa |
85 | Idiopathic interstitial pneumonia |
285 | Fanconi anemia |
60 | Aplastic anemia |
19 | Lysosomal storage disease |
284 | Diamond-Blackfan anemia |
11 | Myasthenia gravis |
160 | Congenital ichthyosis |
164 | Oculocutaneous albinism |
44 | Wegener granulomatosis |
222 | Primary nephrotic syndrome |
228 | Bronchiolitis obliterans |
283 | Acquired pure red cell aplasia |
95 | Autoimmune hepatitis |
28 | Systemic amyloidosis |
43 | Microscopic polyangiitis |
6 | Parkinson disease |
62 | Paroxysmal nocturnal hemoglobinuria |
286 | Hereditary sideroblastic anemia |
151 | Rasmussen encephalitis |
38 | Stevens-Johnson syndrome |
66 | IgA nephropathy |
302 | Leber hereditary optic neuropathy |
39 | Toxic epidermal necrolysis |
326 | Osteopetrosis |
299 | Cystic fibrosis |
36 | Epidermolysis bullosa |
37 | Generalised pustular psoriasis |
274 | Osteogenesis Imperfecta |
113 | Muscular dystrophy |
2 | Amyotrophic lateral sclerosis |
226 | Interstitial cystitis with Hunners ulcer |
26 | HTLV-1-associated myelopathy |
64 | Thrombotic thrombocytopenic purpura |
331 | Idiopathic multicentric castleman disease |
20 | Adrenoleukodystrophy |
227 | Osler disease |
224 | Purpura nephritis |
61 | Autoimmune hemolytic anemia |
58 | Hypertrophic cardiomyopathy |
270 | Chronic recurrent multifocal osteomyelitis |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
35 | Pemphigus |
86 | Pulmonary arterial hypertension |
63 | Idiopathic thrombocytopenic purpura |
106 | Cryopyrin-associated periodic syndrome |
300 | IgG4-related disease |
256 | Muscle glycogenosis |
268 | Nakajo-Nishimura syndrome |
325 | Hereditary autoinflammatory syndrome |
158 | Tuberous sclerosis |
34 | Neurofibromatosis |
211 | Hypoplastic left heart syndrome |
16 | Crow-Fukase syndrome |
90 | Retinitis pigmentosa |
298 | Hereditary pancreatitis |
47 | Buerger disease |
266 | Familial mediterranean fever |
25 | Progressive multifocal leukoencephalopathy |
229 | Autoimmune pulmonary alveolar proteinosis |
172 | Hypophosphatasia |
235 | Hypoparathyroidism |
10 | Charcot-Marie-Tooth disease |
15 | Inclusion body myositis |
108 | TNF receptor-associated periodic syndrome |
267 | Hyper-IgD syndrome |
54 | Adult still disease |
52 | Mixed connective tissue disease |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |