2. Amyotrophic lateral sclerosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 645 / Drugs : 589 - (DrugBank : 163) / Drug target genes : 150 - Drug target pathways : 225
Amyotrophic lateral sclerosis 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) |
---|---|
2 | Amyotrophic lateral sclerosis |
13 | Multiple sclerosis/Neuromyelitis optica |
6 | Parkinson disease |
96 | Crohn disease |
46 | Malignant rheumatoid arthritis |
156 | Rett syndrome |
8 | Huntington disease |
5 | Progressive supranuclear palsy |
97 | Ulcerative colitis |
206 | Fragile X syndrome |
17 | Multiple system atrophy |
3 | Spinal muscular atrophy |
140 | Dorabe syndrome |
21 | Mitochondrial disease |
144 | Lennox-Gastaut syndrome |
65 | Primary immunodeficiency |
34 | Neurofibromatosis |
70 | Spinal stenosis |
18 | Spinocerebellar degeneration |
85 | Idiopathic interstitial pneumonia |
193 | Prader-Willi syndrome |
226 | Interstitial cystitis with Hunners ulcer |
36 | Epidermolysis bullosa |
49 | Systemic lupus erythematosus |
299 | Cystic fibrosis |
113 | Muscular dystrophy |
158 | Tuberous sclerosis |
26 | HTLV-1-associated myelopathy |
51 | Scleroderma |
86 | Pulmonary arterial hypertension |
145 | West syndrome |
98 | Eosinophilic gastrointestinal disease |
22 | Moyamoya disease |
201 | Angelman syndrome |
205 | Fragile X syndrome related disease |
127 | Frontotemporal lobar degeneration |
28 | Systemic amyloidosis |
231 | Alpha-1-antitrypsin deficiency |
84 | Sarcoidosis |
78 | Hypopituitarism |
298 | Hereditary pancreatitis |
107 | Juvenile idiopathic arthritis |
56 | Behcet disease |
152 | PCDH19 related syndrome |
42 | Polyarteritis nodosa |
296 | Biliary atresia |
331 | Idiopathic multicentric castleman disease |
90 | Retinitis pigmentosa |
63 | Idiopathic thrombocytopenic purpura |
75 | Cushing disease |
203 | 22q11.2 deletion syndrome |
53 | Sjogren syndrome |
222 | Primary nephrotic syndrome |
272 | Fibrodysplasia ossificans progressiva |
4 | Primary lateral sclerosis |
38 | Stevens-Johnson syndrome |
62 | Paroxysmal nocturnal hemoglobinuria |
58 | Hypertrophic cardiomyopathy |
254 | Porphyria |
265 | Lipodystrophy |
266 | Familial mediterranean fever |
11 | Myasthenia gravis |
149 | Hemiconvulsion hemiplegia epilepsy syndrome |
93 | Primary biliary cholangitis |
256 | Muscle glycogenosis |
1 | Spinal and bulbar muscular atrophy |
283 | Acquired pure red cell aplasia |
155 | Acquired aphasia with convulsive disorder |
50 | Dermatomyositis |
210 | Single Ventricle |
162 | Pemphigoid |
164 | Oculocutaneous albinism |
215 | Tetralogy of Fallot |
285 | Fanconi anemia |
66 | IgA nephropathy |
35 | Pemphigus |
95 | Autoimmune hepatitis |
89 | Lymphangioleiomyomatosis |
39 | Toxic epidermal necrolysis |
233 | Wolfram syndrome |
19 | Lysosomal storage disease |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
61 | Autoimmune hemolytic anemia |
7 | Corticobasal degeneration |
60 | Aplastic anemia |
102 | Rubinstein-Taybi syndrome |
284 | Diamond-Blackfan anemia |
20 | Adrenoleukodystrophy |
224 | Purpura nephritis |
236 | Pseudohypoparathyroidism |
118 | Myelomeningocele |
151 | Rasmussen encephalitis |
45 | Eosinophilic granulomatosis with Polyangiitis |
228 | Bronchiolitis obliterans |
169 | Menkes disease |
170 | Occipital horn syndrome |
74 | Prolactin secreting pituitary adenoma |
302 | Leber hereditary optic neuropathy |
294 | Congenital diaphragmatic hernia |
10 | Charcot-Marie-Tooth disease |
269 | Pyogenic arthritis |
55 | Relapsing polychondritis |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
83 | Addison disease |
76 | Pituitary gonadotropin secretion hyperthyroidism |
64 | Thrombotic thrombocytopenic purpura |
41 | Giant cell arteritis |
271 | Ankylosing spondylitis |
168 | Ehlers-Danlos syndrome |
57 | Idiopathic dilated cardiomyopathy |
309 | Progressive myoclonus epilepsy |
246 | Methylmalonic acidemia |
227 | Osler disease |
160 | Congenital ichthyosis |
94 | Primary sclerosing cholangitis |
40 | Takayasu arteritis |
300 | IgG4-related disease |
15 | Inclusion body myositis |
157 | Sturge-Weber syndrome |
286 | Hereditary sideroblastic anemia |
81 | Congenital adrenal hyperplasia |
279 | Huge venous malformation with cervical, oral and pharyngeal diffuse lesion |
187 | Kabuki syndrome |
323 | Aromatic L-amino acid decarboxylase deficiency |
288 | Autoimmune acquired coagulation factor deficiency |
43 | Microscopic polyangiitis |
274 | Osteogenesis Imperfecta |
67 | Polycystic kidney disease |
71 | Idiopathic osteonecrosis of the femoral head |
212 | Tricuspid atresia |
77 | Growth hormone secreting pituitary adenoma |
282 | Congenital dyserythropoietic anemia |
307 | Canavan disease |
278 | Huge lymphatic malformation with cervicofacial lesion |
16 | Crow-Fukase syndrome |
211 | Hypoplastic left heart syndrome |
326 | Osteopetrosis |
47 | Buerger disease |
114 | Non-dystrophic myotonia syndrome |
14 | Chronic inflammatory demyelinating polyneuropathy |
225 | Congenital nephrogenic diabetes insipidus |
37 | Generalised pustular psoriasis |
44 | Wegener granulomatosis |
301 | Macular dystrophy |
179 | Williams syndrome |
87 | Pulmonary veno-occlusive disease |
106 | Cryopyrin-associated periodic syndrome |
251 | Urea cycle disorder |
137 | Focal cortical dysplasia |
192 | Cockayne syndrome |
277 | Lymphangiomatosis |
281 | Klippel-Trenaunay-Weber syndrome |
111 | Congenital myopathy |
54 | Adult still disease |
191 | Werner syndrome |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |