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DOID:0110127 - Bardet-Biedl syndrome 5
Disease Ontology Definition:A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the BBS5 gene on chromosome 2q31.
Synonyms: BBS5
Echinobase Genes
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
Bardet-Biedl syndrome (is_a)