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Bardet-Biedl syndrome 16

MONDO:0014444

Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the SDCCAG8 gene.

Also known as: BBS16, Bardet-Biedl syndrome 16, Bardet-Biedl syndrome caused by mutation in SDCCAG8, Bardet-Biedl syndrome type 16, SDCCAG8 Bardet-Biedl syndrome

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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