193. Prader-Willi syndrome Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 113 / Drugs : 111 - (DrugBank : 26) / Drug target genes : 48 - Drug target pathways : 102
Prader-Willi 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 |
---|---|---|
193 | Prader-Willi syndrome | - |
6 | Parkinson disease | 42.594 |
13 | Multiple sclerosis/Neuromyelitis optica | 42.270 |
140 | Dorabe syndrome | 35.982 |
144 | Lennox-Gastaut syndrome | 35.826 |
156 | Rett syndrome | 33.094 |
97 | Ulcerative colitis | 30.888 |
2 | Amyotrophic lateral sclerosis | 27.628 |
8 | Huntington disease | 25.929 |
206 | Fragile X syndrome | 23.208 |
17 | Multiple system atrophy | 22.437 |
96 | Crohn disease | 21.086 |
298 | Hereditary pancreatitis | 20.767 |
5 | Progressive supranuclear palsy | 19.572 |
3 | Spinal muscular atrophy | 19.507 |
70 | Spinal stenosis | 19.492 |
18 | Spinocerebellar degeneration | 19.336 |
36 | Epidermolysis bullosa | 17.517 |
46 | Malignant rheumatoid arthritis | 17.284 |
272 | Fibrodysplasia ossificans progressiva | 17.195 |
231 | Alpha-1-antitrypsin deficiency | 16.059 |
152 | PCDH19 related syndrome | 16.000 |
145 | West syndrome | 15.468 |
84 | Sarcoidosis | 15.013 |
158 | Tuberous sclerosis | 14.790 |
22 | Moyamoya disease | 13.840 |
34 | Neurofibromatosis | 13.711 |
155 | Acquired aphasia with convulsive disorder | 13.582 |
205 | Fragile X syndrome related disease | 13.373 |
201 | Angelman syndrome | 13.005 |
75 | Cushing disease | 12.831 |
21 | Mitochondrial disease | 11.898 |
98 | Eosinophilic gastrointestinal disease | 10.366 |
296 | Biliary atresia | 9.948 |
203 | 22q11.2 deletion syndrome | 6.353 |
226 | Interstitial cystitis with Hunners ulcer | 6.065 |
168 | Ehlers-Danlos syndrome | 5.658 |
86 | Pulmonary arterial hypertension | 5.265 |
58 | Hypertrophic cardiomyopathy | 3.636 |
81 | Congenital adrenal hyperplasia | 3.353 |
113 | Muscular dystrophy | 3.323 |
114 | Non-dystrophic myotonia syndrome | 3.309 |
157 | Sturge-Weber syndrome | 3.263 |
127 | Frontotemporal lobar degeneration | 3.256 |
51 | Scleroderma | 3.212 |
167 | Marfan syndrome | 2.745 |
1 | Spinal and bulbar muscular atrophy | 2.745 |
10 | Charcot-Marie-Tooth disease | 2.540 |
67 | Polycystic kidney disease | 2.073 |
38 | Stevens-Johnson syndrome | 1.993 |
90 | Retinitis pigmentosa | 1.824 |
107 | Juvenile idiopathic arthritis | 1.774 |
256 | Muscle glycogenosis | 1.731 |
28 | Systemic amyloidosis | 1.601 |
78 | Hypopituitarism | 1.428 |
50 | Dermatomyositis | 1.368 |
72 | Pituitary ADH secretion disorder | 1.039 |
137 | Focal cortical dysplasia | 1.000 |
192 | Cockayne syndrome | 1.000 |
277 | Lymphangiomatosis | 1.000 |
281 | Klippel-Trenaunay-Weber syndrome | 1.000 |
191 | Werner syndrome | 1.000 |