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Summary Literature (3)
DOID:0060232 - branchiootic syndrome


Disease Ontology Definition:A syndrome characterized by malformations of the outer, middle and inner ear and branchial and renal malformations. Mutations of the EYA1, SIX1 and SIX5 genes are associated with the syndrome.

Synonyms: BO syndrome, BOR, branchiootic dysplasia

In OMIM:
OMIM:608389 - BRANCHIOOTIC SYNDROME 3; BOS3

In Mondo Disease Ontology:
MONDO:0018878 - branchiootic syndrome

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

Xenbase Genes : eya1, six1

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