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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

Referenced OMIM:
OMIM:612291 - JOUBERT SYNDROME 8; JBTS8

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : arl13b

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Joubert syndrome (is_a)


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