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Summary Literature (0)
DOID:14702 - branchiootorenal syndrome

Disease Ontology Definition:A syndrome characterized by branchial arch anomalies (branchial fistulas, clefts, or cysts), hearing impairment, structural defects of the outer, middle, and inner ear, and renal abnormalities.

Synonyms: branchiootorenal dysplasia, Branchio-otorenal dysplasia, Branchio-Oto-renal syndrome, Melnick-Fraser syndrome, Melnick-Fraser syndrome (disorder)

Xenbase Genes : eya1, six1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007029 - branchio-oto-renal 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)