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Bardet-Biedl syndrome 3

MONDO:0010832

Also known as: BBS3, Bardet-Biedl syndrome 3, Bardet-Biedl syndrome type 3

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

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Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Human disease (14) Bardet-Biedl syndrome (6) Autosomal recessive disease (4) Ciliopathy (2) Disease by molecular mechanism (2) Disease of genetic or genomic mechanism (2) ARL6-related ciliopathy (0)
Trials to join now! 1 Completed 1
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  • Scientists hunt for drug targets in rare kidney disorder

    Knowledge-focused Recruiting now

    This 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

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