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Summary Literature (0)
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

Xenbase Genes : arl13b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012855 - Joubert syndrome 8

MIM:
MIM:612291 - JOUBERT SYNDROME 8; JBTS8

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

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