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:0050691 - branchiooculofacial syndrome

Disease Ontology Definition:A syndrome that is characterized by low birth weight and growth retardation, bilateral branchial clefts.

Synonyms:

Xenbase Genes : tfap2a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007235 - branchiooculofacial syndrome


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

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