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Summary Literature (0)
OMIM:613090 - BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4B

Xenbase Genes: clcnkb

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000909 - Bartter disease type 4B
MONDO:0015231 - Bartter syndrome
MONDO:0019524 - infantile Bartter syndrome with sensorineural deafness