Joubert syndrome 10

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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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ofd1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010431 - Joubert syndrome 10

MONDO:0010431 - Joubert syndrome 10

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view

Parent(s): Joubert syndrome (is_a), X-linked recessive disease (is_a)