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DO Term : Bartter disease type 4a [DOID:0110145] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32.

synonyms:
ICD10CM:E26.8,
BARTS4A,
602522,
Bartter syndrome type 4a,
neonatal Bartter syndrome with sensorineural deafness,
BSND,
OMIM:602522

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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