206. Fragile X syndrome Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 108 / Drugs : 91 - (DrugBank : 36) / Drug target genes : 52 - Drug target pathways : 77
Fragile X syndrome 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 |
---|---|---|
206 | Fragile X syndrome | - |
6 | Parkinson disease | 50.607 |
13 | Multiple sclerosis/Neuromyelitis optica | 45.299 |
8 | Huntington disease | 44.316 |
2 | Amyotrophic lateral sclerosis | 42.572 |
17 | Multiple system atrophy | 36.430 |
5 | Progressive supranuclear palsy | 36.011 |
97 | Ulcerative colitis | 33.960 |
18 | Spinocerebellar degeneration | 33.600 |
156 | Rett syndrome | 32.297 |
46 | Malignant rheumatoid arthritis | 29.053 |
3 | Spinal muscular atrophy | 28.157 |
21 | Mitochondrial disease | 26.505 |
140 | Dorabe syndrome | 26.324 |
96 | Crohn disease | 23.956 |
144 | Lennox-Gastaut syndrome | 23.520 |
193 | Prader-Willi syndrome | 23.208 |
70 | Spinal stenosis | 22.727 |
22 | Moyamoya disease | 22.095 |
205 | Fragile X syndrome related disease | 18.947 |
158 | Tuberous sclerosis | 18.473 |
145 | West syndrome | 16.735 |
152 | PCDH19 related syndrome | 16.000 |
201 | Angelman syndrome | 15.818 |
34 | Neurofibromatosis | 14.345 |
203 | 22q11.2 deletion syndrome | 14.000 |
298 | Hereditary pancreatitis | 13.252 |
231 | Alpha-1-antitrypsin deficiency | 12.171 |
272 | Fibrodysplasia ossificans progressiva | 11.670 |
155 | Acquired aphasia with convulsive disorder | 10.953 |
75 | Cushing disease | 10.459 |
36 | Epidermolysis bullosa | 10.408 |
98 | Eosinophilic gastrointestinal disease | 10.182 |
296 | Biliary atresia | 9.752 |
84 | Sarcoidosis | 9.539 |
113 | Muscular dystrophy | 8.708 |
127 | Frontotemporal lobar degeneration | 7.259 |
118 | Myelomeningocele | 6.238 |
4 | Primary lateral sclerosis | 6.140 |
78 | Hypopituitarism | 6.046 |
169 | Menkes disease | 4.222 |
170 | Occipital horn syndrome | 4.222 |
179 | Williams syndrome | 4.222 |
215 | Tetralogy of Fallot | 4.214 |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion | 3.954 |
49 | Systemic lupus erythematosus | 3.649 |
288 | Autoimmune acquired coagulation factor deficiency | 3.277 |
299 | Cystic fibrosis | 3.244 |
86 | Pulmonary arterial hypertension | 3.204 |
226 | Interstitial cystitis with Hunners ulcer | 3.125 |
11 | Myasthenia gravis | 3.000 |
171 | Wilson disease | 3.000 |
323 | Aromatic L-amino acid decarboxylase deficiency | 3.000 |
65 | Primary immunodeficiency | 2.250 |
85 | Idiopathic interstitial pneumonia | 2.182 |
337 | Homocystinuria | 2.000 |
120 | Hereditary dystonia | 2.000 |
77 | Growth hormone secreting pituitary adenoma | 2.000 |
254 | Porphyria | 1.657 |
67 | Polycystic kidney disease | 1.509 |
271 | Ankylosing spondylitis | 1.447 |
187 | Kabuki syndrome | 1.358 |
58 | Hypertrophic cardiomyopathy | 1.333 |
212 | Tricuspid atresia | 1.229 |
225 | Congenital nephrogenic diabetes insipidus | 1.219 |
210 | Single Ventricle | 1.172 |
149 | Hemiconvulsion hemiplegia epilepsy syndrome | 1.168 |
57 | Idiopathic dilated cardiomyopathy | 1.111 |
251 | Urea cycle disorder | 1.037 |
309 | Progressive myoclonus epilepsy | 1.037 |