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Bardet-Biedl syndrome 16

rare

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

Identifiers
MONDO:0014444 OMIM:615993
Part of
Bardet-Biedl syndromeSDCCAG8-related ciliopathy
Also known as
Bardet-Biedl syndrome caused by mutation in SDCCAG8 · Bardet-Biedl syndrome type 16 · BBS16 · SDCCAG8 Bardet-Biedl syndrome

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