222. Primary nephrotic syndrome Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 310 / Drugs : 295 - (DrugBank : 117) / Drug target genes : 63 - Drug target pathways : 194
Primary nephrotic 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 |
---|---|---|
222 | Primary nephrotic syndrome | - |
13 | Multiple sclerosis/Neuromyelitis optica | 26.997 |
46 | Malignant rheumatoid arthritis | 19.418 |
85 | Idiopathic interstitial pneumonia | 19.374 |
51 | Scleroderma | 18.802 |
66 | IgA nephropathy | 18.088 |
49 | Systemic lupus erythematosus | 16.573 |
65 | Primary immunodeficiency | 16.466 |
2 | Amyotrophic lateral sclerosis | 13.337 |
96 | Crohn disease | 12.441 |
58 | Hypertrophic cardiomyopathy | 12.158 |
164 | Oculocutaneous albinism | 12.029 |
6 | Parkinson disease | 11.301 |
50 | Dermatomyositis | 11.096 |
228 | Bronchiolitis obliterans | 11.055 |
113 | Muscular dystrophy | 10.131 |
97 | Ulcerative colitis | 10.098 |
107 | Juvenile idiopathic arthritis | 9.704 |
11 | Myasthenia gravis | 9.370 |
61 | Autoimmune hemolytic anemia | 9.254 |
62 | Paroxysmal nocturnal hemoglobinuria | 9.103 |
284 | Diamond-Blackfan anemia | 8.815 |
19 | Lysosomal storage disease | 8.622 |
300 | IgG4-related disease | 8.596 |
224 | Purpura nephritis | 8.596 |
93 | Primary biliary cholangitis | 8.536 |
41 | Giant cell arteritis | 7.789 |
60 | Aplastic anemia | 7.728 |
86 | Pulmonary arterial hypertension | 7.595 |
283 | Acquired pure red cell aplasia | 7.494 |
84 | Sarcoidosis | 7.280 |
269 | Pyogenic arthritis | 7.213 |
95 | Autoimmune hepatitis | 7.204 |
285 | Fanconi anemia | 7.203 |
26 | HTLV-1-associated myelopathy | 7.187 |
34 | Neurofibromatosis | 7.134 |
55 | Relapsing polychondritis | 7.082 |
256 | Muscle glycogenosis | 7.060 |
102 | Rubinstein-Taybi syndrome | 7.000 |
162 | Pemphigoid | 6.800 |
53 | Sjogren syndrome | 6.773 |
45 | Eosinophilic granulomatosis with Polyangiitis | 6.284 |
274 | Osteogenesis Imperfecta | 6.260 |
331 | Idiopathic multicentric castleman disease | 6.092 |
151 | Rasmussen encephalitis | 6.000 |
89 | Lymphangioleiomyomatosis | 5.657 |
44 | Wegener granulomatosis | 5.621 |
90 | Retinitis pigmentosa | 5.484 |
20 | Adrenoleukodystrophy | 5.440 |
35 | Pemphigus | 5.440 |
271 | Ankylosing spondylitis | 5.182 |
160 | Congenital ichthyosis | 5.164 |
43 | Microscopic polyangiitis | 5.021 |
302 | Leber hereditary optic neuropathy | 5.000 |
63 | Idiopathic thrombocytopenic purpura | 4.931 |
42 | Polyarteritis nodosa | 4.855 |
28 | Systemic amyloidosis | 4.785 |
233 | Wolfram syndrome | 4.747 |
39 | Toxic epidermal necrolysis | 4.747 |
56 | Behcet disease | 4.739 |
64 | Thrombotic thrombocytopenic purpura | 4.525 |
234 | Peroxisomal disease (except Adrenoleukodystrophy) | 4.418 |
218 | Alport syndrome | 4.235 |
299 | Cystic fibrosis | 4.156 |
158 | Tuberous sclerosis | 4.028 |
127 | Frontotemporal lobar degeneration | 3.730 |
38 | Stevens-Johnson syndrome | 3.695 |
226 | Interstitial cystitis with Hunners ulcer | 3.533 |
36 | Epidermolysis bullosa | 3.346 |
286 | Hereditary sideroblastic anemia | 3.279 |
40 | Takayasu arteritis | 3.273 |
3 | Spinal muscular atrophy | 3.217 |
94 | Primary sclerosing cholangitis | 3.086 |
109 | Atypical hemolytic uremic syndrome | 3.000 |
210 | Single Ventricle | 2.787 |
227 | Osler disease | 2.689 |
5 | Progressive supranuclear palsy | 2.390 |
14 | Chronic inflammatory demyelinating polyneuropathy | 2.322 |
251 | Urea cycle disorder | 2.287 |
298 | Hereditary pancreatitis | 2.098 |
337 | Homocystinuria | 2.000 |
257 | Hepatic glycogenosis | 2.000 |
282 | Congenital dyserythropoietic anemia | 2.000 |
139 | Congenital cerebral hypomyelination | 2.000 |
98 | Eosinophilic gastrointestinal disease | 1.861 |
16 | Crow-Fukase syndrome | 1.859 |
326 | Osteopetrosis | 1.844 |
78 | Hypopituitarism | 1.789 |
215 | Tetralogy of Fallot | 1.685 |
225 | Congenital nephrogenic diabetes insipidus | 1.672 |
15 | Inclusion body myositis | 1.621 |
83 | Addison disease | 1.574 |
81 | Congenital adrenal hyperplasia | 1.508 |
67 | Polycystic kidney disease | 1.444 |
229 | Autoimmune pulmonary alveolar proteinosis | 1.355 |
80 | Resistance to thyroid hormone | 1.355 |
8 | Huntington disease | 1.320 |
212 | Tricuspid atresia | 1.217 |
17 | Multiple system atrophy | 1.122 |
75 | Cushing disease | 1.114 |
79 | Homozygous familial hypercholesterolemia | 1.098 |
288 | Autoimmune acquired coagulation factor deficiency | 1.093 |
106 | Cryopyrin-associated periodic syndrome | 1.033 |
71 | Idiopathic osteonecrosis of the femoral head | 1.033 |
167 | Marfan syndrome | 1.003 |
277 | Lymphangiomatosis | 1.000 |
281 | Klippel-Trenaunay-Weber syndrome | 1.000 |
108 | TNF receptor-associated periodic syndrome | 1.000 |
267 | Hyper-IgD syndrome | 1.000 |
52 | Mixed connective tissue disease | 1.000 |
220 | Rapidly progressive glomerulonephritis | 1.000 |
30 | Distal myopathy | 1.000 |
137 | Focal cortical dysplasia | 1.000 |
192 | Cockayne syndrome | 1.000 |