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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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  • Global PCD data pool aims to unlock secrets of rare lung disease

    Knowledge-focused Ongoing

    This study collects medical information from 3400 people with primary ciliary dyskinesia (PCD) around the world. Researchers will look at symptoms, lung function, growth, and test results to better understand how the disease affects people over time. The goal is to learn more abo…

    Sponsor: University of Bern • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:59 UTC

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