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Summary Literature (0)
OMIM:602522 - BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4A


Xenbase Genes: clcnkb, bsnd

Human Disease Resource: OMIM

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