respiratory system disorder autosomal recessive disease cystic fibrosis DOID:1485 NANDO:1201021 CF MEDGEN:41393 mucoviscidosis NCIT:C2975 NANDO:2200205 SCTID:190905008 OMIM:219700 GARD:6233 MedDRA:10011762 NANDO:2100035 pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis NANDO:1200922 Orphanet:586 NORD:1026 ICD9:277.0 cystic fibrosis lung disease, modifier of MESH:D003550 icd11.foundation:514403112 ICD10CM:E84 UMLS:C0010674 Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity. cystic fibrosis