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Disease Ontology Browser
Bartter disease type 3 (DOID:0110144)
Alliance: disease page
Synonyms: BARTS3; Bartter syndrome type 3; classic Bartter syndrome
Alt IDs: OMIM:607364, ICD10CM:E26.8
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory