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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: 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


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

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