Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:602522 - BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4A

Xenbase Genes: clcnkb, bsnd

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011242 - Bartter disease type 4A
MONDO:0015231 - Bartter syndrome
MONDO:0019524 - Bartter syndrome type 4

Disease Ontology (DO):
DOID:0110145 - Bartter disease type 4a