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Summary Literature (1)
DOID:0050691 - branchiooculofacial syndrome


Disease Ontology Definition:An autosomal dominant disease that is characterized by low birth weight and growth retardation, bilateral branchial clefts.

Synonyms:

Referenced OMIM:
OMIM:113620 - BRANCHIOOCULOFACIAL SYNDROME; BOFS

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tfap2a

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a)


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