34. Neurofibromatosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 133 / Drugs : 186 - (DrugBank : 67) / Drug target genes : 79 - Drug target pathways : 190
Neurofibromatosis 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) |
---|---|
34 | Neurofibromatosis |
13 | Multiple sclerosis/Neuromyelitis optica |
46 | Malignant rheumatoid arthritis |
2 | Amyotrophic lateral sclerosis |
6 | Parkinson disease |
331 | Idiopathic multicentric castleman disease |
28 | Systemic amyloidosis |
51 | Scleroderma |
84 | Sarcoidosis |
85 | Idiopathic interstitial pneumonia |
96 | Crohn disease |
5 | Progressive supranuclear palsy |
8 | Huntington disease |
231 | Alpha-1-antitrypsin deficiency |
22 | Moyamoya disease |
298 | Hereditary pancreatitis |
97 | Ulcerative colitis |
152 | PCDH19 related syndrome |
65 | Primary immunodeficiency |
158 | Tuberous sclerosis |
3 | Spinal muscular atrophy |
36 | Epidermolysis bullosa |
26 | HTLV-1-associated myelopathy |
70 | Spinal stenosis |
89 | Lymphangioleiomyomatosis |
21 | Mitochondrial disease |
206 | Fragile X syndrome |
193 | Prader-Willi syndrome |
18 | Spinocerebellar degeneration |
201 | Angelman syndrome |
272 | Fibrodysplasia ossificans progressiva |
140 | Dorabe syndrome |
256 | Muscle glycogenosis |
145 | West syndrome |
144 | Lennox-Gastaut syndrome |
205 | Fragile X syndrome related disease |
156 | Rett syndrome |
98 | Eosinophilic gastrointestinal disease |
86 | Pulmonary arterial hypertension |
17 | Multiple system atrophy |
155 | Acquired aphasia with convulsive disorder |
56 | Behcet disease |
296 | Biliary atresia |
266 | Familial mediterranean fever |
75 | Cushing disease |
58 | Hypertrophic cardiomyopathy |
49 | Systemic lupus erythematosus |
42 | Polyarteritis nodosa |
113 | Muscular dystrophy |
222 | Primary nephrotic syndrome |
102 | Rubinstein-Taybi syndrome |
107 | Juvenile idiopathic arthritis |
228 | Bronchiolitis obliterans |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
127 | Frontotemporal lobar degeneration |
164 | Oculocutaneous albinism |
93 | Primary biliary cholangitis |
35 | Pemphigus |
210 | Single Ventricle |
233 | Wolfram syndrome |
87 | Pulmonary veno-occlusive disease |
226 | Interstitial cystitis with Hunners ulcer |
38 | Stevens-Johnson syndrome |
90 | Retinitis pigmentosa |
227 | Osler disease |
11 | Myasthenia gravis |
279 | Huge venous malformation with cervical, oral and pharyngeal diffuse lesion |
171 | Wilson disease |
323 | Aromatic L-amino acid decarboxylase deficiency |
168 | Ehlers-Danlos syndrome |
1 | Spinal and bulbar muscular atrophy |
162 | Pemphigoid |
50 | Dermatomyositis |
10 | Charcot-Marie-Tooth disease |
215 | Tetralogy of Fallot |
333 | Hutchinson-Gilford syndrome |
53 | Sjogren syndrome |
60 | Aplastic anemia |
337 | Homocystinuria |
41 | Giant cell arteritis |
67 | Polycystic kidney disease |
149 | Hemiconvulsion hemiplegia epilepsy syndrome |
271 | Ankylosing spondylitis |
114 | Non-dystrophic myotonia syndrome |
270 | Chronic recurrent multifocal osteomyelitis |
88 | Chronic thromboembolic pulmonary hypertension |
172 | Hypophosphatasia |
25 | Progressive multifocal leukoencephalopathy |
118 | Myelomeningocele |
212 | Tricuspid atresia |
78 | Hypopituitarism |
285 | Fanconi anemia |
169 | Menkes disease |
170 | Occipital horn syndrome |
283 | Acquired pure red cell aplasia |
45 | Eosinophilic granulomatosis with Polyangiitis |
288 | Autoimmune acquired coagulation factor deficiency |
106 | Cryopyrin-associated periodic syndrome |
251 | Urea cycle disorder |
137 | Focal cortical dysplasia |
192 | Cockayne syndrome |
277 | Lymphangiomatosis |
281 | Klippel-Trenaunay-Weber syndrome |
108 | TNF receptor-associated periodic syndrome |
267 | Hyper-IgD syndrome |