| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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 | https://www.disgenet.org/browser/0/1/0/C4273131 |
| Similar Terms | |
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5 genes associated with the disease Branchiootic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
