298. Hereditary pancreatitis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 95 / Drugs : 148 - (DrugBank : 51) / Drug target genes : 53 - Drug target pathways : 142
Hereditary pancreatitis 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 |
---|---|---|
298 | Hereditary pancreatitis | - |
13 | Multiple sclerosis/Neuromyelitis optica | 37.764 |
6 | Parkinson disease | 36.742 |
46 | Malignant rheumatoid arthritis | 32.310 |
97 | Ulcerative colitis | 31.508 |
96 | Crohn disease | 31.090 |
70 | Spinal stenosis | 30.751 |
36 | Epidermolysis bullosa | 23.640 |
231 | Alpha-1-antitrypsin deficiency | 22.594 |
140 | Dorabe syndrome | 21.205 |
144 | Lennox-Gastaut syndrome | 21.053 |
193 | Prader-Willi syndrome | 20.767 |
156 | Rett syndrome | 19.595 |
2 | Amyotrophic lateral sclerosis | 18.082 |
158 | Tuberous sclerosis | 17.220 |
272 | Fibrodysplasia ossificans progressiva | 17.126 |
34 | Neurofibromatosis | 16.713 |
152 | PCDH19 related syndrome | 16.000 |
84 | Sarcoidosis | 15.819 |
8 | Huntington disease | 15.723 |
145 | West syndrome | 15.389 |
98 | Eosinophilic gastrointestinal disease | 14.815 |
22 | Moyamoya disease | 13.755 |
205 | Fragile X syndrome related disease | 13.305 |
206 | Fragile X syndrome | 13.252 |
201 | Angelman syndrome | 12.954 |
21 | Mitochondrial disease | 12.846 |
18 | Spinocerebellar degeneration | 11.958 |
3 | Spinal muscular atrophy | 11.181 |
155 | Acquired aphasia with convulsive disorder | 10.993 |
296 | Biliary atresia | 10.868 |
75 | Cushing disease | 10.547 |
226 | Interstitial cystitis with Hunners ulcer | 10.430 |
51 | Scleroderma | 9.751 |
5 | Progressive supranuclear palsy | 9.405 |
17 | Multiple system atrophy | 7.760 |
86 | Pulmonary arterial hypertension | 7.416 |
10 | Charcot-Marie-Tooth disease | 6.148 |
58 | Hypertrophic cardiomyopathy | 5.846 |
107 | Juvenile idiopathic arthritis | 5.642 |
271 | Ankylosing spondylitis | 5.434 |
38 | Stevens-Johnson syndrome | 4.830 |
113 | Muscular dystrophy | 3.908 |
81 | Congenital adrenal hyperplasia | 3.340 |
299 | Cystic fibrosis | 3.282 |
28 | Systemic amyloidosis | 3.116 |
168 | Ehlers-Danlos syndrome | 2.987 |
256 | Muscle glycogenosis | 2.960 |
50 | Dermatomyositis | 2.929 |
53 | Sjogren syndrome | 2.751 |
1 | Spinal and bulbar muscular atrophy | 2.736 |
251 | Urea cycle disorder | 2.292 |
85 | Idiopathic interstitial pneumonia | 2.208 |
222 | Primary nephrotic syndrome | 2.098 |
43 | Microscopic polyangiitis | 2.089 |
337 | Homocystinuria | 2.000 |
282 | Congenital dyserythropoietic anemia | 2.000 |
19 | Lysosomal storage disease | 1.995 |
65 | Primary immunodeficiency | 1.811 |
167 | Marfan syndrome | 1.781 |
45 | Eosinophilic granulomatosis with Polyangiitis | 1.730 |
114 | Non-dystrophic myotonia syndrome | 1.730 |
41 | Giant cell arteritis | 1.647 |
15 | Inclusion body myositis | 1.647 |
67 | Polycystic kidney disease | 1.519 |
35 | Pemphigus | 1.501 |
127 | Frontotemporal lobar degeneration | 1.477 |
40 | Takayasu arteritis | 1.377 |
310 | Congenital anomalies syndrome | 1.358 |
42 | Polyarteritis nodosa | 1.343 |
49 | Systemic lupus erythematosus | 1.298 |
300 | IgG4-related disease | 1.288 |
225 | Congenital nephrogenic diabetes insipidus | 1.226 |
56 | Behcet disease | 1.101 |
95 | Autoimmune hepatitis | 1.080 |
94 | Primary sclerosing cholangitis | 1.080 |
235 | Hypoparathyroidism | 1.038 |
71 | Idiopathic osteonecrosis of the femoral head | 1.038 |
44 | Wegener granulomatosis | 1.006 |
220 | Rapidly progressive glomerulonephritis | 1.000 |
30 | Distal myopathy | 1.000 |