|
DOID:0110139 - Bardet-Biedl syndrome 17
Disease Ontology Definition:A Bardet-Biedl syndrome that has material basis in homozygous or compound heterozygous mutation in the LZTFL1 gene on chromosome 3p21.
Synonyms: BBS17,
Echinobase Genes :
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)