has modifier syndromic disease respiratory system disease ciliopathy primary ciliary dyskinesia DOID:0050144 DOID:9562 Dextrocardia bronchiectasis and sinusitis Dextrocardia-bronchiectasis-sinusitis syndrome Editor note: we deliberately merge two MESHes here GARD:0004484 GARD:0006815 ICD10:Q34.8 ICS Immotile cilia syndrome, Kartagener type Kartagener syndrome Kartagener's syndrome MESH:D002925 MESH:D007619 MONDO:0016575 MedDRA:10069713 NCIT:C84797 OMIMPS:244400 Orphanet:244 PCD Primary ciliary dyskinesia (PCD) is 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). Primary ciliary dyskinesia and situs inversus Primary ciliary dyskinesia, Kartagener type SCTID:42402006 SCTID:86204009 Siewert syndrome UMLS:C0008780 bronchiectasis, chronic sinusitis and dextrocardia syndrome ciliary dyskinesia primary ciliary motility disorder immotile ciliary syndrome kartageners syndrome male infertility due to sperm motility disorder rare