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Summary Literature (0)
DOID:0110981 - Joubert syndrome 10


Disease Ontology Definition:A Joubert syndrome that has_material_basis_in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.

Synonyms: JBTS10


In Mondo Disease Ontology:
MONDO:0010431 - Joubert syndrome 10

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

Xenbase Genes : ofd1

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