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Echinobase
Summary Literature (0)
DOID:0110144 - Bartter disease type 3

Disease Ontology Definition:A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36.

Synonyms: BARTS3, Bartter syndrome type 3, classic Bartter syndrome,

Echinobase Genes :


OMIM:
MIM:607364 - bartter syndrome, type 3

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)