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Bartter Disease Type 4B (MONDO:0000909)

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

Overview

Category

Ontology ID

Internal:3182

Synonyms

BARTS4B

Bartter disease type 4B

Bartter syndrome, type 4B

Bartter syndrome, infantile, with sensorineural deafness

Bartter syndrome, type 4B, neonatal, with sensorineural deafness

Mapped terms

DOID:0110146

GARD:0015612

MEDGEN:934772

OMIM:613090

UMLS:C4310805

Child terms

Unknown children.