Bardet-Biedl syndrome 16

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: sdccag8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014444 - Bardet-Biedl syndrome 16

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)