PedAM
Pediatric Disease Annotations & Medicines
| Disease | interstitial lung disease |
| Phenotype | C1800706|idiopathic pulmonary fibrosis |
| Sentences | 4 |
| PubMedID- 20600766 | idiopathic pulmonary fibrosis (ipf), one of the most common interstitial lung diseases, is caused by accumulation of fibroblasts in lungs. |
| PubMedID- 26317335 | idiopathic pulmonary fibrosis (ipf), one of the most severe interstitial lung diseases, is a progressive fibrotic disorder of unknown etiology. |
| PubMedID- 26317679 | The distinct genetic architecture of pulmonary fibrosis in ssc-associated interstitial lung disease compared with idiopathic pulmonary fibrosis is noteworthy, supporting a distinct genetic risk of these two forms of lung fibrosis and suggesting that fibrosis might be the result of different pathogenic mechanisms, with a more immune-driven cause in ssc [78]. |
| PubMedID- 24051272 | Introduction: idiopathic pulmonary fibrosis (ipf) is one of the most frequent interstitial lung disease. |
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