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 might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Drug repositionability
ID | Diseases (Sorted by drug repositionability) |
---|---|
193 | Prader-Willi syndrome |
6 | Parkinson disease |
13 | Multiple sclerosis/Neuromyelitis optica |
140 | Dorabe syndrome |
144 | Lennox-Gastaut syndrome |
156 | Rett syndrome |
97 | Ulcerative colitis |
2 | Amyotrophic lateral sclerosis |
8 | Huntington disease |
206 | Fragile X syndrome |
17 | Multiple system atrophy |
96 | Crohn disease |
298 | Hereditary pancreatitis |
5 | Progressive supranuclear palsy |
3 | Spinal muscular atrophy |
70 | Spinal stenosis |
18 | Spinocerebellar degeneration |
36 | Epidermolysis bullosa |
46 | Malignant rheumatoid arthritis |
272 | Fibrodysplasia ossificans progressiva |
231 | Alpha-1-antitrypsin deficiency |
152 | PCDH19 related syndrome |
145 | West syndrome |
84 | Sarcoidosis |
158 | Tuberous sclerosis |
22 | Moyamoya disease |
34 | Neurofibromatosis |
155 | Acquired aphasia with convulsive disorder |
205 | Fragile X syndrome related disease |
201 | Angelman syndrome |
75 | Cushing disease |
21 | Mitochondrial disease |
98 | Eosinophilic gastrointestinal disease |
296 | Biliary atresia |
203 | 22q11.2 deletion syndrome |
226 | Interstitial cystitis with Hunners ulcer |
168 | Ehlers-Danlos syndrome |
86 | Pulmonary arterial hypertension |
58 | Hypertrophic cardiomyopathy |
81 | Congenital adrenal hyperplasia |
113 | Muscular dystrophy |
114 | Non-dystrophic myotonia syndrome |
157 | Sturge-Weber syndrome |
127 | Frontotemporal lobar degeneration |
51 | Scleroderma |
167 | Marfan syndrome |
1 | Spinal and bulbar muscular atrophy |
10 | Charcot-Marie-Tooth disease |
67 | Polycystic kidney disease |
38 | Stevens-Johnson syndrome |
90 | Retinitis pigmentosa |
107 | Juvenile idiopathic arthritis |
256 | Muscle glycogenosis |
28 | Systemic amyloidosis |
78 | Hypopituitarism |
50 | Dermatomyositis |
72 | Pituitary ADH secretion disorder |
137 | Focal cortical dysplasia |
192 | Cockayne syndrome |
277 | Lymphangiomatosis |
281 | Klippel-Trenaunay-Weber syndrome |
191 | Werner syndrome |