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DO Term : branchiootic syndrome [DOID:0060232] Disease Ontology
Namespace  disease_ontology Obsolete  false
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.
  • synonyms:
  • GARD:10148,
  • OMIM:608389,
  • ICD10CM:Q87.0,
  • BO syndrome,
  • branchiootic dysplasia,
  • 602588,
  • 608389,
  • ORDO:52429,
  • OMIM:120502,
  • MESH:C537104,
  • BOR,
  • OMIM:602588,
  • 120502
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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