86. Pulmonary arterial hypertension Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 1,205 / Drugs : 684 - (DrugBank : 124) / Drug target genes : 100 - Drug target pathways : 193
Pulmonary arterial hypertension 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) |
---|---|
86 | Pulmonary arterial hypertension |
13 | Multiple sclerosis/Neuromyelitis optica |
6 | Parkinson disease |
2 | Amyotrophic lateral sclerosis |
225 | Congenital nephrogenic diabetes insipidus |
46 | Malignant rheumatoid arthritis |
51 | Scleroderma |
114 | Non-dystrophic myotonia syndrome |
85 | Idiopathic interstitial pneumonia |
90 | Retinitis pigmentosa |
230 | Alveolar hypoventilation syndrome |
96 | Crohn disease |
58 | Hypertrophic cardiomyopathy |
67 | Polycystic kidney disease |
299 | Cystic fibrosis |
97 | Ulcerative colitis |
113 | Muscular dystrophy |
115 | Hereditary periodic paralysis |
154 | Epilepsy with continuous spikes and waves during slow sleep |
226 | Interstitial cystitis with Hunners ulcer |
89 | Lymphangioleiomyomatosis |
88 | Chronic thromboembolic pulmonary hypertension |
127 | Frontotemporal lobar degeneration |
34 | Neurofibromatosis |
28 | Systemic amyloidosis |
70 | Spinal stenosis |
81 | Congenital adrenal hyperplasia |
8 | Huntington disease |
49 | Systemic lupus erythematosus |
65 | Primary immunodeficiency |
210 | Single Ventricle |
222 | Primary nephrotic syndrome |
298 | Hereditary pancreatitis |
156 | Rett syndrome |
256 | Muscle glycogenosis |
84 | Sarcoidosis |
155 | Acquired aphasia with convulsive disorder |
5 | Progressive supranuclear palsy |
167 | Marfan syndrome |
53 | Sjogren syndrome |
19 | Lysosomal storage disease |
140 | Dorabe syndrome |
17 | Multiple system atrophy |
107 | Juvenile idiopathic arthritis |
168 | Ehlers-Danlos syndrome |
57 | Idiopathic dilated cardiomyopathy |
98 | Eosinophilic gastrointestinal disease |
193 | Prader-Willi syndrome |
1 | Spinal and bulbar muscular atrophy |
211 | Hypoplastic left heart syndrome |
74 | Prolactin secreting pituitary adenoma |
66 | IgA nephropathy |
218 | Alport syndrome |
83 | Addison disease |
35 | Pemphigus |
144 | Lennox-Gastaut syndrome |
227 | Osler disease |
87 | Pulmonary veno-occlusive disease |
215 | Tetralogy of Fallot |
280 | Huge arteriovenous malformation with cervicofacial or limb lesion |
254 | Porphyria |
296 | Biliary atresia |
11 | Myasthenia gravis |
10 | Charcot-Marie-Tooth disease |
15 | Inclusion body myositis |
285 | Fanconi anemia |
278 | Huge lymphatic malformation with cervicofacial lesion |
206 | Fragile X syndrome |
271 | Ankylosing spondylitis |
331 | Idiopathic multicentric castleman disease |
288 | Autoimmune acquired coagulation factor deficiency |
75 | Cushing disease |
231 | Alpha-1-antitrypsin deficiency |
169 | Menkes disease |
170 | Occipital horn syndrome |
50 | Dermatomyositis |
36 | Epidermolysis bullosa |
26 | HTLV-1-associated myelopathy |
38 | Stevens-Johnson syndrome |
300 | IgG4-related disease |
78 | Hypopituitarism |
41 | Giant cell arteritis |
233 | Wolfram syndrome |
149 | Hemiconvulsion hemiplegia epilepsy syndrome |
158 | Tuberous sclerosis |
251 | Urea cycle disorder |
309 | Progressive myoclonus epilepsy |
71 | Idiopathic osteonecrosis of the femoral head |
3 | Spinal muscular atrophy |
22 | Moyamoya disease |
118 | Myelomeningocele |
77 | Growth hormone secreting pituitary adenoma |
337 | Homocystinuria |
257 | Hepatic glycogenosis |
282 | Congenital dyserythropoietic anemia |
63 | Idiopathic thrombocytopenic purpura |
228 | Bronchiolitis obliterans |
301 | Macular dystrophy |
157 | Sturge-Weber syndrome |
166 | Pseudoxanthoma elasticum |
294 | Congenital diaphragmatic hernia |
224 | Purpura nephritis |
64 | Thrombotic thrombocytopenic purpura |
265 | Lipodystrophy |
60 | Aplastic anemia |
76 | Pituitary gonadotropin secretion hyperthyroidism |
47 | Buerger disease |
94 | Primary sclerosing cholangitis |
162 | Pemphigoid |
164 | Oculocutaneous albinism |
310 | Congenital anomalies syndrome |
229 | Autoimmune pulmonary alveolar proteinosis |
102 | Rubinstein-Taybi syndrome |
284 | Diamond-Blackfan anemia |
20 | Adrenoleukodystrophy |
56 | Behcet disease |
43 | Microscopic polyangiitis |
61 | Autoimmune hemolytic anemia |
212 | Tricuspid atresia |
272 | Fibrodysplasia ossificans progressiva |
21 | Mitochondrial disease |
7 | Corticobasal degeneration |
179 | Williams syndrome |
106 | Cryopyrin-associated periodic syndrome |
91 | Budd-Chiari syndrome |
283 | Acquired pure red cell aplasia |
137 | Focal cortical dysplasia |
192 | Cockayne syndrome |
277 | Lymphangiomatosis |
281 | Klippel-Trenaunay-Weber syndrome |
111 | Congenital myopathy |
54 | Adult still disease |
52 | Mixed connective tissue disease |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |