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Disease Ontology Browser
Bartter disease type 2 (DOID:0110143)
Alliance: disease page
Synonyms: BARTS2; Bartter syndrome type 2; Bartter syndrome type 2 antenatal; hyperprostaglandin E syndrome 2; hypokalemic alkalosis with hypercalciuria 2 antenatal
Alt IDs: OMIM:241200, ICD10CM:E26.8
Definition: A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory