About   Help   FAQ
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, MESH:C537104, 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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory