|
DOID:0110998 - Joubert syndrome 3
Disease Ontology Definition:A Joubert syndrome that has_material_basis_in homozygous mutation in the AHI1 gene on chromosome 6q23.3.
Synonyms: JBTS3
Echinobase Genes

MIM:608629 - joubert syndrome 3; jbts3 |
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)