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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

MIM:
MIM:113620 - BRANCHIOOCULOFACIAL SYNDROME; BOFS

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)