FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term branchiootic syndrome ID (Ontology) DOID:0060232 (Human Disease)
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.
Also Known As "BO syndrome" ; "BOR" ; "branchiootic dysplasia"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 branchiootic syndrome       2      1
 for disease ribbon | branchiootic syndrome       2       --
 model of | branchiootic syndrome       2       --
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       |__branchiootic syndrome  3 rec.
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Synonyms
  • "BO syndrome" EXACT
    "BOR" EXACT OMO:0003012
    "branchiootic dysplasia" EXACT
Secondary IDs
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GARD:10148
ICD10CM:Q87.0
MESH:C537104
MIM:120502
MIM:602588
MIM:608389
ORDO:52429