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Summary Literature (0)
DOID:0110124 - Bardet-Biedl syndrome 2

Disease Ontology Definition:A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the BBS2 gene on chromosome 16q13.

Synonyms: BBS2

Xenbase Genes : bbs2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014432 - Bardet-Biedl syndrome 2


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

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