Congenital tracheomalacia is a rare condition where the trachea is soft and flexible causing the tracheal wall to collapse when exhaling, coughing or crying, that usually presents in infancy, and that is characterized by stridor and noisy breathing or upper respiratory infections. Tracheomalacia improves by the age of 18-24 months. [ Orphanet:95430 ]
Synonyms: congenital major airway collapse congenital tracheomalacia Congenital Tracheomalacia
Term information
- MEDGEN:215296 (MONDO:equivalentTo)
- NORD:2028 (MONDO:NORD)
- icd11.foundation:1616705280 (https://orcid.org/0000-0001-5208-3432)
- SCTID:95467005 (MONDO:equivalentTo)
- MedDRA:10010654 (Orphanet:95430/e)
- MESH:D055090 (https://orcid.org/0000-0003-1967-3726)
- DOID:0060313 (MONDO:equivalentTo)
- Orphanet:95430 (MONDO:equivalentTo)
- HP:0002779 (MONDO:otherHierarchy)
- NCIT:C98634 (MONDO:equivalentTo)
- UMLS:C0948187 (MONDO:equivalentTo)
- ICD9:748.3 (MONDO:relatedTo)
- NANDO:2200195 (https://orcid.org/0000-0003-0011-764X)
- GARD:10515 (MONDO:GARD)
ordo_disorder, gard_rare, otar, rare, ordo_morphological_anomaly, nord_rare, orphanet_rare
http://purl.obolibrary.org/obo/DOID_0060313
http://identifiers.org/snomedct/95467005
http://identifiers.org/medgen/215296
http://identifiers.org/mesh/D055090
http://purl.obolibrary.org/obo/NCIT_C98634
http://linkedlifedata.com/resource/umls/id/C0948187
http://www.orpha.net/ORDO/Orphanet_95430