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DO Term : Bartter disease type 4b [DOID:0110146] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes.

synonyms:
OMIM:613090,
613090,
ICD10CM:E26.8,
BARTS4B,
neonatal Bartter syndrome type 4B with sensorineural deafness,
Bartter syndrome, type 4b, digenic

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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