Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0110145 - Bartter disease type 4a

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

Synonyms: BARTS4A, Bartter syndrome type 4a , neonatal Bartter syndrome with sensorineural deafness, Bartter syndrome type 4a, BSND

Echinobase Genes :


MIM:
MIM:602522 - bartter syndrome, type 4a

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Bartter disease (is_a)