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DOID:0111000 - Joubert syndrome 5
Disease Ontology Definition:A Joubert syndrome that has_material_basis_in mutation in the CEP290 gene on chromosome 12q21.
Synonyms: JBTS5
Echinobase Genes

MIM:610188 - joubert syndrome 5; jbts5 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Joubert syndrome (is_a)