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, 6 tagged with Primary ciliary dyskinesia 1 itself.

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Where it sits in the disease tree

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↑ Primary ciliary dyskinesia (34)

Including sub-types (6) Tagged with Primary ciliary dyskinesia 1 (6)

Trials to join now! 4 Not yet finished but already full! 1 Completed 1

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

Primary ciliary dyskinesia 1

Where it sits in the disease tree

Study aims to map respiratory attacks in rare lung disease