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.
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Can a simple breath test diagnose diseases in children?
Knowledge-focused Recruiting nowThis study aims to see if analyzing the chemicals in a child's breath can help diagnose and monitor diseases like asthma, neurological disorders, and type 1 diabetes. Researchers will collect breath samples from up to 3,600 children and teens to find patterns linked to these cond…
Sponsor: University Children's Hospital Basel • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:30 UTC
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Scientists hunt for drug targets in rare kidney disorder
Knowledge-focused Recruiting nowThis study looks at the genetic causes of nephronophthisis, a rare kidney disease that leads to kidney failure before age 20. Researchers will collect urine and blood samples from 310 patients and healthy relatives to study cells and identify potential drug targets. The goal is t…
Phase: NA • Sponsor: Imagine Institute • Aim: Knowledge-focused
Last updated Jun 26, 2026 14:13 UTC