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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

Xenbase Genes : clcnkb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000909 - Bartter disease type 4B


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)