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DO Term : branchiootorenal syndrome 2 [DOID:0111424] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A branchiootorenal syndrome that has_material_basis_in heterozygous mutation in the SIX5 gene on chromosome 19q13.32.

synonyms:
610896,
BOR2,
OMIM:610896

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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