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DOID:0110143 - Bartter disease type 2
Disease Ontology Definition:A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
Synonyms: BARTS2, Bartter syndrome type 2, Bartter syndrome type 2 antenatal, hyperprostaglandin E syndrome 2, hypokalemic alkalosis with hypercalciuria 2 antenatal,
Echinobase Genes

OMIM:241200 - bartter syndrome, antenatal, type 2 |
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)