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Summary Literature (1)
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: First AND second branchial arch syndrome, HEMIFACIAL MICROSOMIA, OAV (oculoauriculovertebral) dysplasia, Facio-auriculo-vertebral spectrum (disorder), First arch syndrome (disorder), Otomandibular dysostosis (disorder), Facio-auriculo-vertebral spectrum, First arch syndrome, Otomandibular dysostosis

Xenbase Genes : myt1

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

MIM:
MIM:164210 - CRANIOFACIAL MICROSOMIA 1; CFM1

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

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