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PedAM

Pediatric Disease Annotations & Medicines




Disease collagen disease
Phenotype C1800706|idiopathic pulmonary fibrosis
Sentences 3
PubMedID- 25307273 Background and aims: information regarding autoimmune symptoms that do not meet the diagnostic criteria for connective tissue disease in patients with idiopathic pulmonary fibrosis (ipf) is limited.
PubMedID- 23997057 Pulmonary hypertension (ph) is a common complication of interstitial lung diseases (ilds), particularly in idiopathic pulmonary fibrosis and ild associated with connective tissue disease.
PubMedID- 23247773 idiopathic pulmonary fibrosis (ipf), fibrosis associated with connective tissue disease, asbestosis, end-stage sarcoidosis or chronic hypersensitivity pneumonitis (hp) may present with lower zone, subpleural reticular pattern associated with honeycombing.

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