Joubert syndrome 18

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Summary

Literature (0)

DOID:0110987 - Joubert syndrome 18

Disease Ontology Definition:A Joubert syndrome that has_material_basis_in homozygous mutation in the TCTN3 gene on chromosome 10q24.

Synonyms: JBTS18,

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

: tctn3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013896 - Joubert syndrome 18

MONDO:0013896 - Joubert syndrome 18

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

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

Parent(s): Joubert syndrome (is_a)