Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
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, Facio-auriculo-vertebral spectrum (disorder), First AND second branchial arch syndrome, First arch syndrome, First arch syndrome (disorder), HEMIFACIAL MICROSOMIA, OAV (oculoauriculovertebral) dysplasia, Otomandibular dysostosis, Otomandibular dysostosis (disorder)

Xenbase Genes : myt1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008112 - obsolete Goldenhar syndrome

OMIM:
OMIM:164210 - CRANIOFACIAL MICROSOMIA; CFM

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndrome (is_a)