90. Retinitis pigmentosa Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 147 / Drugs : 176 - (DrugBank : 43) / Drug target genes : 49 - Drug target pathways : 110
Retinitis pigmentosa 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) |
---|---|
90 | Retinitis pigmentosa |
13 | Multiple sclerosis/Neuromyelitis optica |
6 | Parkinson disease |
86 | Pulmonary arterial hypertension |
2 | Amyotrophic lateral sclerosis |
115 | Hereditary periodic paralysis |
154 | Epilepsy with continuous spikes and waves during slow sleep |
230 | Alveolar hypoventilation syndrome |
114 | Non-dystrophic myotonia syndrome |
225 | Congenital nephrogenic diabetes insipidus |
155 | Acquired aphasia with convulsive disorder |
26 | HTLV-1-associated myelopathy |
97 | Ulcerative colitis |
65 | Primary immunodeficiency |
102 | Rubinstein-Taybi syndrome |
299 | Cystic fibrosis |
226 | Interstitial cystitis with Hunners ulcer |
39 | Toxic epidermal necrolysis |
85 | Idiopathic interstitial pneumonia |
164 | Oculocutaneous albinism |
96 | Crohn disease |
222 | Primary nephrotic syndrome |
58 | Hypertrophic cardiomyopathy |
140 | Dorabe syndrome |
4 | Primary lateral sclerosis |
302 | Leber hereditary optic neuropathy |
233 | Wolfram syndrome |
5 | Progressive supranuclear palsy |
50 | Dermatomyositis |
151 | Rasmussen encephalitis |
46 | Malignant rheumatoid arthritis |
51 | Scleroderma |
62 | Paroxysmal nocturnal hemoglobinuria |
224 | Purpura nephritis |
331 | Idiopathic multicentric castleman disease |
20 | Adrenoleukodystrophy |
34 | Neurofibromatosis |
113 | Muscular dystrophy |
160 | Congenital ichthyosis |
283 | Acquired pure red cell aplasia |
286 | Hereditary sideroblastic anemia |
127 | Frontotemporal lobar degeneration |
49 | Systemic lupus erythematosus |
89 | Lymphangioleiomyomatosis |
11 | Myasthenia gravis |
7 | Corticobasal degeneration |
323 | Aromatic L-amino acid decarboxylase deficiency |
107 | Juvenile idiopathic arthritis |
284 | Diamond-Blackfan anemia |
53 | Sjogren syndrome |
38 | Stevens-Johnson syndrome |
269 | Pyogenic arthritis |
17 | Multiple system atrophy |
74 | Prolactin secreting pituitary adenoma |
64 | Thrombotic thrombocytopenic purpura |
70 | Spinal stenosis |
63 | Idiopathic thrombocytopenic purpura |
45 | Eosinophilic granulomatosis with Polyangiitis |
215 | Tetralogy of Fallot |
144 | Lennox-Gastaut syndrome |
95 | Autoimmune hepatitis |
81 | Congenital adrenal hyperplasia |
55 | Relapsing polychondritis |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
256 | Muscle glycogenosis |
3 | Spinal muscular atrophy |
309 | Progressive myoclonus epilepsy |
66 | IgA nephropathy |
201 | Angelman syndrome |
212 | Tricuspid atresia |
274 | Osteogenesis Imperfecta |
227 | Osler disease |
40 | Takayasu arteritis |
61 | Autoimmune hemolytic anemia |
42 | Polyarteritis nodosa |
8 | Huntington disease |
326 | Osteopetrosis |
166 | Pseudoxanthoma elasticum |
36 | Epidermolysis bullosa |
149 | Hemiconvulsion hemiplegia epilepsy syndrome |
193 | Prader-Willi syndrome |
167 | Marfan syndrome |
285 | Fanconi anemia |
41 | Giant cell arteritis |
162 | Pemphigoid |
228 | Bronchiolitis obliterans |
93 | Primary biliary cholangitis |
158 | Tuberous sclerosis |
56 | Behcet disease |
156 | Rett syndrome |
60 | Aplastic anemia |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
118 | Myelomeningocele |
28 | Systemic amyloidosis |
19 | Lysosomal storage disease |
288 | Autoimmune acquired coagulation factor deficiency |
169 | Menkes disease |
170 | Occipital horn syndrome |
254 | Porphyria |
37 | Generalised pustular psoriasis |
202 | Smith-Magenis syndrome |
78 | Hypopituitarism |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |