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Primary ciliary dyskinesia 1

MONDO:0009484

Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI1 gene.

Also known as: CILD1, DNAI1 primary ciliary dyskinesia, ciliary dyskinesia, primary, type 1, primary ciliary dyskinesia 1, primary ciliary dyskinesia caused by mutation in DNAI1, primary ciliary dyskinesia type 1, Kartagener syndrome, PCD

6 clinical trials for this condition and its sub-types.

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Broader categories

Disease (717) Hereditary disease (188) Respiratory system disorder (146) Primary ciliary dyskinesia (34) Syndromic disease (25) Human disease (15) Ciliopathy (2) Disease by molecular mechanism (2) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)
Trials to join now! 4 Not yet finished but already full! 1 Completed 1
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  • Study aims to map respiratory attacks in rare lung disease

    Knowledge-focused Completed

    This completed study followed 105 children and adults with primary ciliary dyskinesia (PCD), a rare lung condition, to track how their breathing and quality of life change during respiratory flare-ups. Researchers measured lung function, symptoms, and daily impacts to gather info…

    Sponsor: University of North Carolina, Chapel Hill • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:03 UTC

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