|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||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. (Human Disease Ontology, DOID_0060232)|
|Downloads & Tools|
1 genes associated with the Branchiootic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|EYA1||EYA transcriptional coactivator and phosphatase 1|