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 might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Drug repositionability
ID | Diseases (Sorted by drug repositionability) |
---|---|
298 | Hereditary pancreatitis |
13 | Multiple sclerosis/Neuromyelitis optica |
6 | Parkinson disease |
46 | Malignant rheumatoid arthritis |
97 | Ulcerative colitis |
96 | Crohn disease |
70 | Spinal stenosis |
36 | Epidermolysis bullosa |
231 | Alpha-1-antitrypsin deficiency |
140 | Dorabe syndrome |
144 | Lennox-Gastaut syndrome |
193 | Prader-Willi syndrome |
156 | Rett syndrome |
2 | Amyotrophic lateral sclerosis |
158 | Tuberous sclerosis |
272 | Fibrodysplasia ossificans progressiva |
34 | Neurofibromatosis |
152 | PCDH19 related syndrome |
84 | Sarcoidosis |
8 | Huntington disease |
145 | West syndrome |
98 | Eosinophilic gastrointestinal disease |
22 | Moyamoya disease |
205 | Fragile X syndrome related disease |
206 | Fragile X syndrome |
201 | Angelman syndrome |
21 | Mitochondrial disease |
18 | Spinocerebellar degeneration |
3 | Spinal muscular atrophy |
155 | Acquired aphasia with convulsive disorder |
296 | Biliary atresia |
75 | Cushing disease |
226 | Interstitial cystitis with Hunners ulcer |
51 | Scleroderma |
5 | Progressive supranuclear palsy |
17 | Multiple system atrophy |
86 | Pulmonary arterial hypertension |
10 | Charcot-Marie-Tooth disease |
58 | Hypertrophic cardiomyopathy |
107 | Juvenile idiopathic arthritis |
271 | Ankylosing spondylitis |
38 | Stevens-Johnson syndrome |
113 | Muscular dystrophy |
81 | Congenital adrenal hyperplasia |
299 | Cystic fibrosis |
28 | Systemic amyloidosis |
168 | Ehlers-Danlos syndrome |
256 | Muscle glycogenosis |
50 | Dermatomyositis |
53 | Sjogren syndrome |
1 | Spinal and bulbar muscular atrophy |
251 | Urea cycle disorder |
85 | Idiopathic interstitial pneumonia |
222 | Primary nephrotic syndrome |
43 | Microscopic polyangiitis |
337 | Homocystinuria |
282 | Congenital dyserythropoietic anemia |
19 | Lysosomal storage disease |
65 | Primary immunodeficiency |
167 | Marfan syndrome |
45 | Eosinophilic granulomatosis with Polyangiitis |
114 | Non-dystrophic myotonia syndrome |
41 | Giant cell arteritis |
15 | Inclusion body myositis |
67 | Polycystic kidney disease |
35 | Pemphigus |
127 | Frontotemporal lobar degeneration |
40 | Takayasu arteritis |
310 | Congenital anomalies syndrome |
42 | Polyarteritis nodosa |
49 | Systemic lupus erythematosus |
300 | IgG4-related disease |
225 | Congenital nephrogenic diabetes insipidus |
56 | Behcet disease |
95 | Autoimmune hepatitis |
94 | Primary sclerosing cholangitis |
235 | Hypoparathyroidism |
71 | Idiopathic osteonecrosis of the femoral head |
44 | Wegener granulomatosis |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |