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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: Branchio-Oto-renal syndrome, Branchio-otorenal dysplasia, branchiootorenal dysplasia, Melnick-Fraser syndrome (disorder), Melnick-Fraser syndrome
Echinobase Genes
:
eya1,
six1
| MIM:113650 - branchiootorenal syndrome 1; bor1 |
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)