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Bardet-Biedl syndrome 1

rare

A Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBS1 gene on chromosome 11q13.

Identifiers
MONDO:0008854 OMIM:209900
Part of
BBS1-related ciliopathyBardet-Biedl syndrome
Also known as
Bardet-Biedl syndrome 1, modifier of · Bardet-Biedl syndrome type 1 · BBS1

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