17. Multiple system atrophy Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 119 / Drugs : 138 - (DrugBank : 44) / Drug target genes : 59 - Drug target pathways : 111
Multiple system atrophy 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 |
---|---|---|
17 | Multiple system atrophy | - |
6 | Parkinson disease | 56.028 |
2 | Amyotrophic lateral sclerosis | 42.107 |
5 | Progressive supranuclear palsy | 41.368 |
13 | Multiple sclerosis/Neuromyelitis optica | 39.616 |
206 | Fragile X syndrome | 36.430 |
8 | Huntington disease | 34.119 |
46 | Malignant rheumatoid arthritis | 27.900 |
18 | Spinocerebellar degeneration | 27.605 |
97 | Ulcerative colitis | 27.480 |
140 | Dorabe syndrome | 26.929 |
156 | Rett syndrome | 25.596 |
3 | Spinal muscular atrophy | 24.672 |
96 | Crohn disease | 24.407 |
70 | Spinal stenosis | 24.163 |
22 | Moyamoya disease | 23.419 |
193 | Prader-Willi syndrome | 22.437 |
201 | Angelman syndrome | 22.000 |
21 | Mitochondrial disease | 19.334 |
144 | Lennox-Gastaut syndrome | 18.998 |
205 | Fragile X syndrome related disease | 18.797 |
152 | PCDH19 related syndrome | 16.000 |
296 | Biliary atresia | 14.811 |
158 | Tuberous sclerosis | 14.239 |
203 | 22q11.2 deletion syndrome | 14.000 |
98 | Eosinophilic gastrointestinal disease | 13.115 |
145 | West syndrome | 12.458 |
36 | Epidermolysis bullosa | 12.044 |
272 | Fibrodysplasia ossificans progressiva | 11.460 |
4 | Primary lateral sclerosis | 11.161 |
75 | Cushing disease | 10.894 |
155 | Acquired aphasia with convulsive disorder | 10.709 |
231 | Alpha-1-antitrypsin deficiency | 10.694 |
34 | Neurofibromatosis | 10.553 |
215 | Tetralogy of Fallot | 10.158 |
113 | Muscular dystrophy | 10.131 |
84 | Sarcoidosis | 9.836 |
169 | Menkes disease | 9.000 |
170 | Occipital horn syndrome | 9.000 |
127 | Frontotemporal lobar degeneration | 7.930 |
298 | Hereditary pancreatitis | 7.760 |
118 | Myelomeningocele | 6.225 |
86 | Pulmonary arterial hypertension | 6.085 |
57 | Idiopathic dilated cardiomyopathy | 5.623 |
85 | Idiopathic interstitial pneumonia | 4.739 |
78 | Hypopituitarism | 4.238 |
7 | Corticobasal degeneration | 4.197 |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion | 3.902 |
299 | Cystic fibrosis | 3.566 |
11 | Myasthenia gravis | 3.497 |
49 | Systemic lupus erythematosus | 3.375 |
278 | Huge lymphatic malformation with cervicofacial lesion | 3.252 |
288 | Autoimmune acquired coagulation factor deficiency | 3.213 |
323 | Aromatic L-amino acid decarboxylase deficiency | 3.000 |
90 | Retinitis pigmentosa | 2.737 |
167 | Marfan syndrome | 2.705 |
67 | Polycystic kidney disease | 2.513 |
226 | Interstitial cystitis with Hunners ulcer | 2.407 |
309 | Progressive myoclonus epilepsy | 2.287 |
58 | Hypertrophic cardiomyopathy | 2.208 |
210 | Single Ventricle | 2.159 |
164 | Oculocutaneous albinism | 2.079 |
66 | IgA nephropathy | 2.043 |
120 | Hereditary dystonia | 2.000 |
179 | Williams syndrome | 1.923 |
157 | Sturge-Weber syndrome | 1.859 |
74 | Prolactin secreting pituitary adenoma | 1.844 |
254 | Porphyria | 1.618 |
218 | Alport syndrome | 1.574 |
19 | Lysosomal storage disease | 1.432 |
212 | Tricuspid atresia | 1.217 |
222 | Primary nephrotic syndrome | 1.122 |
137 | Focal cortical dysplasia | 1.000 |
192 | Cockayne syndrome | 1.000 |
277 | Lymphangiomatosis | 1.000 |
281 | Klippel-Trenaunay-Weber syndrome | 1.000 |
111 | Congenital myopathy | 1.000 |
52 | Mixed connective tissue disease | 1.000 |