Human genes for branchiootic syndrome
Branchiootic syndrome [DOID:0060232]
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.
Synonyms: branchiootic syndrome, branchiootic disease, branchiootic disorder, branchiootic syndromes, DOID:0060232 ...