84. Sarcoidosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 149 / Drugs : 202 - (DrugBank : 78) / Drug target genes : 66 - Drug target pathways : 169
Sarcoidosis 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) |
---|---|
84 | Sarcoidosis |
13 | Multiple sclerosis/Neuromyelitis optica |
46 | Malignant rheumatoid arthritis |
6 | Parkinson disease |
97 | Ulcerative colitis |
96 | Crohn disease |
296 | Biliary atresia |
51 | Scleroderma |
34 | Neurofibromatosis |
50 | Dermatomyositis |
2 | Amyotrophic lateral sclerosis |
36 | Epidermolysis bullosa |
107 | Juvenile idiopathic arthritis |
152 | PCDH19 related syndrome |
298 | Hereditary pancreatitis |
8 | Huntington disease |
193 | Prader-Willi syndrome |
18 | Spinocerebellar degeneration |
231 | Alpha-1-antitrypsin deficiency |
21 | Mitochondrial disease |
271 | Ankylosing spondylitis |
205 | Fragile X syndrome related disease |
41 | Giant cell arteritis |
53 | Sjogren syndrome |
145 | West syndrome |
70 | Spinal stenosis |
201 | Angelman syndrome |
158 | Tuberous sclerosis |
49 | Systemic lupus erythematosus |
98 | Eosinophilic gastrointestinal disease |
140 | Dorabe syndrome |
144 | Lennox-Gastaut syndrome |
162 | Pemphigoid |
156 | Rett syndrome |
272 | Fibrodysplasia ossificans progressiva |
56 | Behcet disease |
75 | Cushing disease |
22 | Moyamoya disease |
155 | Acquired aphasia with convulsive disorder |
17 | Multiple system atrophy |
206 | Fragile X syndrome |
44 | Wegener granulomatosis |
65 | Primary immunodeficiency |
93 | Primary biliary cholangitis |
3 | Spinal muscular atrophy |
222 | Primary nephrotic syndrome |
86 | Pulmonary arterial hypertension |
164 | Oculocutaneous albinism |
40 | Takayasu arteritis |
256 | Muscle glycogenosis |
58 | Hypertrophic cardiomyopathy |
228 | Bronchiolitis obliterans |
226 | Interstitial cystitis with Hunners ulcer |
5 | Progressive supranuclear palsy |
85 | Idiopathic interstitial pneumonia |
60 | Aplastic anemia |
299 | Cystic fibrosis |
11 | Myasthenia gravis |
43 | Microscopic polyangiitis |
269 | Pyogenic arthritis |
66 | IgA nephropathy |
55 | Relapsing polychondritis |
284 | Diamond-Blackfan anemia |
28 | Systemic amyloidosis |
285 | Fanconi anemia |
19 | Lysosomal storage disease |
88 | Chronic thromboembolic pulmonary hypertension |
106 | Cryopyrin-associated periodic syndrome |
113 | Muscular dystrophy |
94 | Primary sclerosing cholangitis |
265 | Lipodystrophy |
38 | Stevens-Johnson syndrome |
300 | IgG4-related disease |
35 | Pemphigus |
211 | Hypoplastic left heart syndrome |
283 | Acquired pure red cell aplasia |
45 | Eosinophilic granulomatosis with Polyangiitis |
160 | Congenital ichthyosis |
42 | Polyarteritis nodosa |
95 | Autoimmune hepatitis |
168 | Ehlers-Danlos syndrome |
37 | Generalised pustular psoriasis |
47 | Buerger disease |
224 | Purpura nephritis |
1 | Spinal and bulbar muscular atrophy |
331 | Idiopathic multicentric castleman disease |
78 | Hypopituitarism |
10 | Charcot-Marie-Tooth disease |
15 | Inclusion body myositis |
127 | Frontotemporal lobar degeneration |
63 | Idiopathic thrombocytopenic purpura |
62 | Paroxysmal nocturnal hemoglobinuria |
268 | Nakajo-Nishimura syndrome |
325 | Hereditary autoinflammatory syndrome |
263 | Cerebrotendinous xanthomatosis |
266 | Familial mediterranean fever |
114 | Non-dystrophic myotonia syndrome |
270 | Chronic recurrent multifocal osteomyelitis |
218 | Alport syndrome |
83 | Addison disease |
20 | Adrenoleukodystrophy |
171 | Wilson disease |
310 | Congenital anomalies syndrome |
172 | Hypophosphatasia |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
61 | Autoimmune hemolytic anemia |
212 | Tricuspid atresia |
246 | Methylmalonic acidemia |
225 | Congenital nephrogenic diabetes insipidus |
79 | Homozygous familial hypercholesterolemia |
288 | Autoimmune acquired coagulation factor deficiency |
235 | Hypoparathyroidism |
137 | Focal cortical dysplasia |
192 | Cockayne syndrome |
277 | Lymphangiomatosis |
281 | Klippel-Trenaunay-Weber syndrome |
108 | TNF receptor-associated periodic syndrome |
267 | Hyper-IgD syndrome |
317 | Trifunctional protein deficiency |
54 | Adult still disease |
52 | Mixed connective tissue disease |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |