Ciliary dyskinesia, primary, 36, X-linked
MONDO:0010517Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the PIH1D3 gene.
Also known as: CILD36, PIH1D3 primary ciliary dyskinesia, ciliary dyskinesia, primary, 36, X-linked, ciliary dyskinesia, primary, 36, X-linked, X-linked recessive, ciliary dyskinesia, primary, 36, X-linked; CILD36, primary ciliary dyskinesia caused by mutation in PIH1D3, ciliary dyskinesia, primary, 36, with or without situs inversus
7 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
Could a tiny dose of muscle relaxant make lung scopes safer?
Symptom relief CompletedThis study looked at whether giving a low dose of a muscle relaxant (rocuronium) during bronchoscopy—a procedure where a tube is inserted into the lungs—could reduce complications like throat spasms and coughing. 153 adults having elective bronchoscopy were split into two groups:…
Phase: NA • Sponsor: Harbin Medical University • Aim: Symptom relief
Last updated Jun 27, 2026 09:09 UTC
-
Scientists hunt for early warning signs of kidney failure in rare genetic diseases
Knowledge-focused CompletedThis completed study collected blood and urine samples from 240 people with ciliopathies—rare genetic disorders that often lead to kidney failure. Researchers analyzed these samples to find biological markers that could predict how the disease will progress. The goal is to develo…
Phase: NA • Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:29 UTC