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DOID:0111004 - Joubert syndrome 9
Disease Ontology Definition:A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15.
Synonyms: JBTS9,
Xenbase Genes : cc2d2a
MONDO:0012849 - Joubert syndrome 9 |
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)