Primary ciliary dyskinesia
MONDO:0016575A 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).
Also known as: Kartagener syndrome, Kartagener's syndrome, PCD, Dextrocardia bronchiectasis and sinusitis, Dextrocardia-bronchiectasis-sinusitis syndrome, ICS, Immotile cilia syndrome, Kartagener type, Primary ciliary dyskinesia and situs inversus
37 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Primary ciliary dyskinesia 1
(6)
CFAP46-related primary ciliary dyskinesia
(0)
Ciliary discoordination due to random ciliary orientation
(0)
Ciliary dyskinesia, primary, 36, X-linked
(0)
Ciliary dyskinesia, primary, 37
(0)
Ciliary dyskinesia, primary, 38
(0)
Ciliary dyskinesia, primary, 39
(0)
Ciliary dyskinesia, primary, 40
(0)
Ciliary dyskinesia, primary, 41
(0)
Ciliary dyskinesia, primary, 42
(0)
Ciliary dyskinesia, primary, 43
(0)
Ciliary dyskinesia, primary, 44
(0)
Ciliary dyskinesia, primary, 45
(0)
Ciliary dyskinesia, primary, 46
(0)
Ciliary dyskinesia, primary, 47, and lissencephaly
(0)
Ciliary dyskinesia, primary, 48, without situs inversus
(0)
Ciliary dyskinesia, primary, 49, without situs inversus
(0)
Ciliary dyskinesia, primary, 50
(0)
Ciliary dyskinesia, primary, 51
(0)
Ciliary dyskinesia, primary, 52
(0)
Broader categories
Disease
(618)
Hereditary disease
(172)
Respiratory system disorder
(127)
Syndromic disease
(24)
Human disease
(14)
Ciliopathy
(2)
Disease by molecular mechanism
(2)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)