idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause. [ ]
Term info
idiopathic pulmonary fibrosis
- CFA
- UIP
- cryptogenic fibrosing alveolitis
- fibrocystic pulmonary dysplasia
- idiopathic pulmonary fibrosis
- idiopathic pulmonary fibrosis, familial
- usual interstitial pneumonia
gard_rare, ordo_disease
http://purl.obolibrary.org/obo/NCIT_C35715, http://identifiers.org/snomedct/426437004, http://identifiers.org/snomedct/700250006, http://identifiers.org/snomedct/28168000, http://linkedlifedata.com/resource/umls/id/C1800706, http://identifiers.org/snomedct/233721005, http://identifiers.org/snomedct/237121003
http://purl.obolibrary.org/obo/NCIT_C35716, http://identifiers.org/omim/178500, http://identifiers.org/meddra/10021240, http://identifiers.org/mesh/D054990, http://purl.obolibrary.org/obo/DOID_0050156, http://identifiers.org/snomedct/196125002
true
pulmonary fibrosis, idiopathic, familial idiopathic pulmonary fibrosis, Hamman-rich disease, interstitial pneumonitis, usual, fibrosing alveolitis, cryptogenic, IPF, fibrosing alveolitis
https://rarediseases.info.nih.gov/diseases/8609/idiopathic-pulmonary-fibrosis