DISEASES

Disease-gene associations mined from literature

JensenLab

Human genes for branchiootorenal syndrome

Branchiootorenal syndrome [DOID:14702]

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 syndrome,  DOID:14702,  branchiootorenal disease,  branchiootorenal disorder,  branchiootorenal syndromes ...

Linkouts:  OMIM #1 #2