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,
Xenbase Genes : clcnkb
|MONDO:0000909 - Bartter disease type 4B|
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)