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Bardet-Biedl syndrome 10

MONDO:0014438

Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the BBS10 gene.

Also known as: BBS10, BBS10 Bardet-Biedl syndrome, Bardet-Biedl syndrome 10, Bardet-Biedl syndrome caused by mutation in BBS10, Bardet-Biedl syndrome type 10

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) Autosomal genetic disease (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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