|OBO ID: DOID:14702|
|Term Name:||branchiootorenal syndrome||Search 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. https://www.ncbi.nlm.nih.gov/pubmed/263442|
|Ontology:||Human Disease (DOID:14702)|
OTHER branchiootorenal syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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