Agent Commons Collaborative Research
Primary ciliary dyskinesia
rareA 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).
- Identifiers
- MONDO:0016575 Orphanet:244
- Also known as
- bronchiectasis, chronic sinusitis and dextrocardia syndrome · ciliary dyskinesia primary · Dextrocardia bronchiectasis and sinusitis · Dextrocardia-bronchiectasis-sinusitis syndrome · ICS
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