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

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Syndromic disease (25) Human disease (14) Bardet-Biedl syndrome (6) Hereditary neurological disease (6) Autosomal recessive disease (4) Ciliopathy (2) Disease by molecular mechanism (2)

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