A rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower respiratory tract disease. Approximately half of PCD patients have an organ laterality defect (situs inversus totalis or situs ambiguus/heterotaxy). [ Orphanet:244 ]
Synonyms: PCD ciliary motility disorder Kartagener syndrome Kartagener's syndrome immotile ciliary syndrome
Term information
- DOID:0050144 (MONDO:equivalentTo)
- MESH:D002925 (MONDO:equivalentTo)
- NANDO:2200203 (https://orcid.org/0000-0003-0011-764X)
- UMLS:C0008780 (MONDO:equivalentTo)
- NANDO:2200204 (https://orcid.org/0000-0003-0011-764X)
- NORD:1605 (MONDO:NORD)
- DOID:9562 (MONDO:equivalentTo)
- SCTID:42402006 (MONDO:equivalentTo)
- MEDGEN:3467 (MONDO:equivalentTo)
- NCIT:C84797 (MONDO:equivalentTo)
- MedDRA:10069713 (Orphanet:244/e)
- GARD:4484 (MONDO:GARD)
- MESH:D007619 (MONDO:equivalentTo)
- OMIMPS:244400 (MONDO:equivalentTo)
- NANDO:2100034 (https://orcid.org/0000-0003-0011-764X)
- SCTID:86204009 (MONDO:equivalentTo)
- Orphanet:244 (MONDO:equivalentTo)
ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare, clingen
http://www.orpha.net/ORDO/Orphanet_244
http://linkedlifedata.com/resource/umls/id/C0008780
http://identifiers.org/mesh/D002925
http://purl.obolibrary.org/obo/DOID_0050144
http://purl.obolibrary.org/obo/NCIT_C84797
https://omim.org/phenotypicSeries/PS244400
http://identifiers.org/snomedct/86204009
http://identifiers.org/snomedct/42402006
http://identifiers.org/mesh/D007619
http://purl.obolibrary.org/obo/DOID_9562
http://identifiers.org/medgen/3467
bronchiectasis, chronic sinusitis and dextrocardia syndrome
ciliary dyskinesia primary
Dextrocardia bronchiectasis and sinusitis
ICS
Dextrocardia-bronchiectasis-sinusitis syndrome
Immotile cilia syndrome, Kartagener type
Primary ciliary dyskinesia and situs inversus
Siewert syndrome
Primary ciliary dyskinesia, Kartagener type