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Summary Literature (0)
DOID:0110138 - Bardet-Biedl syndrome 16


Disease Ontology Definition:A Bardet-Biedl syndrome that has material basis in homozygous or compound heterozygous mutations in the SDCCAG8 gene on chromosome 1q43.

Synonyms: BBS16

Xenbase Genes : sdccag8

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014444 - Bardet-Biedl syndrome 16


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Bardet-Biedl syndrome (is_a)