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:0110146 - Bartter disease type 4b

Disease Ontology Definition:A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.

Synonyms: BARTS4B, Bartter syndrome, type 4b, digenic, neonatal Bartter syndrome type 4B with sensorineural deafness,

Echinobase Genes :



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

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