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DOID:0110141 - Bardet-Biedl syndrome 19
Disease Ontology Definition:A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the IFT27 gene on chromosome 22q12.
Synonyms: BBS19
Echinobase Genes

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)