PedAM
Pediatric Disease Annotations & Medicines
| Disease | interstitial lung disease |
| Phenotype | C0034069|pulmonary fibrosis |
| Sentences | 8 |
| PubMedID- 26552223 | [computed tomography in evaluating the development of different types of pulmonary fibrosis in patients with interstitial lung diseases]. |
| PubMedID- 20600766 | Idiopathic pulmonary fibrosis (ipf), one of the most common interstitial lung diseases, is caused by accumulation of fibroblasts in lungs. |
| PubMedID- 24860860 | The main indications for ltx in the pediatric population are pulmonary cystic fibrosis, interstitial lung disease associated with pulmonary fibrosis, and congenital vascular disease (4,5). |
| PubMedID- 23668427 | Secondly, there are patients whose predominant symptom is cough but clearly have conditions which are a recognised illness, such as pulmonary fibrosis due to interstitial lung disease or non cystic fibrosis bronchiectasis. |
| PubMedID- 24051272 | Introduction: idiopathic pulmonary fibrosis (ipf) is one of the most frequent interstitial lung disease. |
| PubMedID- 22826322 | interstitial lung disease (ild) with pulmonary fibrosis is an important manifestation in systemic sclerosis (ssc, scleroderma) where it portends a poor prognosis. |
| PubMedID- 21050542 | Objectives: to evaluate an improved quantitative lung fibrosis score based on a computer-aided diagnosis (cad) system that classifies ct pixels with the visual semi-quantitative pulmonary fibrosis score in patients with scleroderma-related interstitial lung disease (ssc-ild). |
| PubMedID- 26317335 | Idiopathic pulmonary fibrosis (ipf), one of the most severe interstitial lung diseases, is a progressive fibrotic disorder of unknown etiology. |
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