299. Cystic fibrosis Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 1,695 / Drugs : 1,527 - (DrugBank : 268) / Drug target genes : 111 - Drug target pathways : 174
Cystic fibrosis 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) |
---|---|
299 | Cystic fibrosis |
13 | Multiple sclerosis/Neuromyelitis optica |
46 | Malignant rheumatoid arthritis |
6 | Parkinson disease |
226 | Interstitial cystitis with Hunners ulcer |
2 | Amyotrophic lateral sclerosis |
63 | Idiopathic thrombocytopenic purpura |
96 | Crohn disease |
97 | Ulcerative colitis |
236 | Pseudohypoparathyroidism |
86 | Pulmonary arterial hypertension |
65 | Primary immunodeficiency |
246 | Methylmalonic acidemia |
265 | Lipodystrophy |
78 | Hypopituitarism |
49 | Systemic lupus erythematosus |
51 | Scleroderma |
113 | Muscular dystrophy |
107 | Juvenile idiopathic arthritis |
21 | Mitochondrial disease |
225 | Congenital nephrogenic diabetes insipidus |
50 | Dermatomyositis |
19 | Lysosomal storage disease |
8 | Huntington disease |
53 | Sjogren syndrome |
20 | Adrenoleukodystrophy |
162 | Pemphigoid |
224 | Purpura nephritis |
271 | Ankylosing spondylitis |
56 | Behcet disease |
58 | Hypertrophic cardiomyopathy |
90 | Retinitis pigmentosa |
164 | Oculocutaneous albinism |
39 | Toxic epidermal necrolysis |
158 | Tuberous sclerosis |
95 | Autoimmune hepatitis |
285 | Fanconi anemia |
74 | Prolactin secreting pituitary adenoma |
64 | Thrombotic thrombocytopenic purpura |
75 | Cushing disease |
98 | Eosinophilic gastrointestinal disease |
84 | Sarcoidosis |
60 | Aplastic anemia |
66 | IgA nephropathy |
302 | Leber hereditary optic neuropathy |
294 | Congenital diaphragmatic hernia |
274 | Osteogenesis Imperfecta |
26 | HTLV-1-associated myelopathy |
210 | Single Ventricle |
41 | Giant cell arteritis |
62 | Paroxysmal nocturnal hemoglobinuria |
326 | Osteopetrosis |
93 | Primary biliary cholangitis |
85 | Idiopathic interstitial pneumonia |
151 | Rasmussen encephalitis |
222 | Primary nephrotic syndrome |
179 | Williams syndrome |
67 | Polycystic kidney disease |
227 | Osler disease |
160 | Congenital ichthyosis |
228 | Bronchiolitis obliterans |
17 | Multiple system atrophy |
5 | Progressive supranuclear palsy |
28 | Systemic amyloidosis |
298 | Hereditary pancreatitis |
206 | Fragile X syndrome |
286 | Hereditary sideroblastic anemia |
234 | Peroxisomal disease (except Adrenoleukodystrophy) |
156 | Rett syndrome |
283 | Acquired pure red cell aplasia |
45 | Eosinophilic granulomatosis with Polyangiitis |
11 | Myasthenia gravis |
301 | Macular dystrophy |
7 | Corticobasal degeneration |
36 | Epidermolysis bullosa |
76 | Pituitary gonadotropin secretion hyperthyroidism |
38 | Stevens-Johnson syndrome |
269 | Pyogenic arthritis |
284 | Diamond-Blackfan anemia |
296 | Biliary atresia |
251 | Urea cycle disorder |
309 | Progressive myoclonus epilepsy |
55 | Relapsing polychondritis |
94 | Primary sclerosing cholangitis |
254 | Porphyria |
77 | Growth hormone secreting pituitary adenoma |
337 | Homocystinuria |
195 | Noonan syndrome |
263 | Cerebrotendinous xanthomatosis |
282 | Congenital dyserythropoietic anemia |
120 | Hereditary dystonia |
70 | Spinal stenosis |
61 | Autoimmune hemolytic anemia |
40 | Takayasu arteritis |
42 | Polyarteritis nodosa |
127 | Frontotemporal lobar degeneration |
288 | Autoimmune acquired coagulation factor deficiency |
15 | Inclusion body myositis |
233 | Wolfram syndrome |
218 | Alport syndrome |
83 | Addison disease |
124 | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
18 | Spinocerebellar degeneration |
4 | Primary lateral sclerosis |
140 | Dorabe syndrome |
37 | Generalised pustular psoriasis |
81 | Congenital adrenal hyperplasia |
187 | Kabuki syndrome |
171 | Wilson disease |
310 | Congenital anomalies syndrome |
229 | Autoimmune pulmonary alveolar proteinosis |
88 | Chronic thromboembolic pulmonary hypertension |
201 | Angelman syndrome |
168 | Ehlers-Danlos syndrome |
79 | Homozygous familial hypercholesterolemia |
256 | Muscle glycogenosis |
106 | Cryopyrin-associated periodic syndrome |
333 | Hutchinson-Gilford syndrome |
238 | Vitamin D-resistant rickets |
72 | Pituitary ADH secretion disorder |
235 | Hypoparathyroidism |
71 | Idiopathic osteonecrosis of the femoral head |
3 | Spinal muscular atrophy |
232 | Carney complex |
111 | Congenital myopathy |
317 | Trifunctional protein deficiency |
191 | Werner syndrome |
290 | Chronic nonspecific multiple ulcers of the small intestine |
220 | Rapidly progressive glomerulonephritis |
30 | Distal myopathy |