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Summary Literature (0)
DOID:0110145 - Bartter disease type 4a


Disease Ontology Definition:A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32.

Synonyms: BARTS4A, BSND, Bartter syndrome type 4a , neonatal Bartter syndrome with sensorineural deafness

Xenbase Genes : bsnd, clcnkb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011242 - Bartter disease type 4a

OMIM:
OMIM:602522 - BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4A

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Bartter disease (is_a)