DOID:2907 - Goldenhar syndrome
Disease Ontology Definition:A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch.
Synonyms: Facio-auriculo-vertebral spectrum (disorder), First AND second branchial arch syndrome, First arch syndrome (disorder), HEMIFACIAL MICROSOMIA, OAV (oculoauriculovertebral) dysplasia, Otomandibular dysostosis (disorder)
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndrome (is_a)