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Disease Ontology Browser
branchiootic syndrome (DOID:0060232)
Alliance: disease page
Synonyms: BO syndrome; BOR; branchiootic dysplasia
Alt IDs: OMIM:120502, OMIM:602588, OMIM:608389, ICD10CM:Q87.0, ORDO:52429
Definition: 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.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory