About   Help   FAQ
Disease Ontology Browser
Bartter disease type 4b (DOID:0110146)
Synonyms: BARTS4B; Bartter syndrome, type 4b, digenic; neonatal Bartter syndrome type 4B with sensorineural deafness
Alt IDs: OMIM:613090, ICD10CM:E26.8
Definition: A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/18/2017
MGI 6.08
The Jackson Laboratory