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Disease Ontology Browser
bronchiectasis (DOID:9563)
Alliance: disease page
Synonyms: Polynesian bronchiectasis
Alt IDs: OMIM:211400, OMIM:613021, OMIM:613071, DOID:11046, DOID:11047, DOID:9571, ICD10CM:J47, ICD9CM:494, MESH:D001987, NCI:C84475, OMIM:PS211400, ORDO:60033, UMLS_CUI:C0006267
Definition: A bronchial disease that is a chronic inflammatory condition of one or more bronchi or bronchioles marked by dilatation and loss of elasticity of the walls resulting from damage to the airway wall leading to the formation of small sacs on the bronchial wall and impairment of cilia mobility in the lung. Inflammation of the bronchial wall increases mucus secretion which serves as a breeding ground for bacteria. Bronchiectasis is caused by repeated respiratory infections, immune deficiency disorders, hereditary disorders (cystic fibrosis or primary ciliary dyskinesia), mechanical factors (inhaled object or a lung tumor) or inhaling toxic substances.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory