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Bardet-Biedl syndrome 11

MONDO:0014439

Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the TRIM32 gene.

Also known as: BBS11, Bardet-Biedl syndrome 11, Bardet-Biedl syndrome caused by mutation in TRIM32, Bardet-Biedl syndrome type 11, TRIM32 Bardet-Biedl syndrome

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

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Syndromic disease (24) Human disease (14) Bardet-Biedl syndrome (6) Hereditary neurological disease (5) Autosomal recessive disease (4) Ciliopathy (2) Disease by molecular mechanism (2)
Trials to join now! 1 Completed 1
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