70. Spinal stenosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 95 / Drugs : 169 - (DrugBank : 61) / Drug target genes : 68 - Drug target pathways : 90
Spinal stenosis 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) |
---|---|
70 | Spinal stenosis |
46 | Malignant rheumatoid arthritis |
6 | Parkinson disease |
13 | Multiple sclerosis/Neuromyelitis optica |
96 | Crohn disease |
298 | Hereditary pancreatitis |
2 | Amyotrophic lateral sclerosis |
97 | Ulcerative colitis |
22 | Moyamoya disease |
5 | Progressive supranuclear palsy |
8 | Huntington disease |
17 | Multiple system atrophy |
231 | Alpha-1-antitrypsin deficiency |
21 | Mitochondrial disease |
206 | Fragile X syndrome |
156 | Rett syndrome |
205 | Fragile X syndrome related disease |
36 | Epidermolysis bullosa |
193 | Prader-Willi syndrome |
140 | Dorabe syndrome |
144 | Lennox-Gastaut syndrome |
3 | Spinal muscular atrophy |
272 | Fibrodysplasia ossificans progressiva |
152 | PCDH19 related syndrome |
18 | Spinocerebellar degeneration |
158 | Tuberous sclerosis |
34 | Neurofibromatosis |
226 | Interstitial cystitis with Hunners ulcer |
201 | Angelman syndrome |
113 | Muscular dystrophy |
296 | Biliary atresia |
84 | Sarcoidosis |
145 | West syndrome |
51 | Scleroderma |
98 | Eosinophilic gastrointestinal disease |
155 | Acquired aphasia with convulsive disorder |
86 | Pulmonary arterial hypertension |
215 | Tetralogy of Fallot |
169 | Menkes disease |
170 | Occipital horn syndrome |
127 | Frontotemporal lobar degeneration |
75 | Cushing disease |
58 | Hypertrophic cardiomyopathy |
78 | Hypopituitarism |
118 | Myelomeningocele |
10 | Charcot-Marie-Tooth disease |
11 | Myasthenia gravis |
85 | Idiopathic interstitial pneumonia |
167 | Marfan syndrome |
288 | Autoimmune acquired coagulation factor deficiency |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
4 | Primary lateral sclerosis |
107 | Juvenile idiopathic arthritis |
168 | Ehlers-Danlos syndrome |
28 | Systemic amyloidosis |
1 | Spinal and bulbar muscular atrophy |
256 | Muscle glycogenosis |
323 | Aromatic L-amino acid decarboxylase deficiency |
57 | Idiopathic dilated cardiomyopathy |
210 | Single Ventricle |
38 | Stevens-Johnson syndrome |
90 | Retinitis pigmentosa |
67 | Polycystic kidney disease |
271 | Ankylosing spondylitis |
81 | Congenital adrenal hyperplasia |
251 | Urea cycle disorder |
235 | Hypoparathyroidism |
49 | Systemic lupus erythematosus |
203 | 22q11.2 deletion syndrome |
337 | Homocystinuria |
299 | Cystic fibrosis |
278 | Huge lymphatic malformation with cervicofacial lesion |
114 | Non-dystrophic myotonia syndrome |
254 | Porphyria |
65 | Primary immunodeficiency |
124 | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
47 | Buerger disease |
53 | Sjogren syndrome |
43 | Microscopic polyangiitis |
300 | IgG4-related disease |
212 | Tricuspid atresia |
45 | Eosinophilic granulomatosis with Polyangiitis |
19 | Lysosomal storage disease |
111 | Congenital myopathy |
317 | Trifunctional protein deficiency |
68 | Ossification of the ligamentum flavum |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |