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DOID:0111003 - Joubert syndrome 8
Disease Ontology Definition:A Joubert syndrome that has_material_basis_in mutation in the ARL13B gene on chromosome 3q11.1-q11.2.
Synonyms: JBTS8
Echinobase Genes

MIM:612291 - joubert syndrome 8; jbts8 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Joubert syndrome (is_a)