congenital pulmonary airway malformation
Go to external page http://purl.obolibrary.org/obo/MONDO_0016580
An abnormality in lung development that is characterized by a multicystic mass resulting from an adenomatous overgrowth of the terminal bronchioles with a consequent reduction of pulmonary alveoli. This anomaly is classified into three types by the cyst size. [ MESH:D015615 ]
Synonyms: CCAM CPAM congenital cystic adenomatoid malformation of lung congenital cystic adenomatoid malformation of the lung congenital cystic adenomatous malformation of the lung congenital cystic disease of the lung
Term information
- SCTID:111318005 (MONDO:equivalentTo)
- UMLS:C0010668 (MONDO:equivalentTo)
- Orphanet:2444 (MONDO:equivalentTo)
- GARD:18772 (MONDO:GARD)
- MESH:D015615 (MONDO:equivalentTo)
- icd11.foundation:2091138945 (https://orcid.org/0000-0002-4142-7153)
- NCIT:C98892 (MONDO:equivalentTo)
- MEDGEN:8225 (MONDO:equivalentTo)
gard_rare, ordo_disorder, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare
https://github.com/monarch-initiative/mondo/issues/6876
https://github.com/monarch-initiative/mondo/issues/4069
https://github.com/monarch-initiative/mondo/issues/6754
http://purl.obolibrary.org/obo/NCIT_C98892
http://identifiers.org/medgen/8225
http://linkedlifedata.com/resource/umls/id/C0010668
http://www.orpha.net/ORDO/Orphanet_2444
http://identifiers.org/snomedct/111318005
http://identifiers.org/mesh/D015615
cystic adenomatoid malformation of lung
congenital cystic adenomatoid malformation