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Echinobase
Summary Literature (0)
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:

Echinobase Genes : tfap2a


OMIM:
MIM:113620 - branchiooculofacial syndrome; bofs

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

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