Branchiootic syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/602588
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Genes

1 genes associated with the Branchiootic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1