Bartter disease type 5

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Echinobase

Summary

Literature (0)

DOID:0110147 - Bartter disease type 5

Disease Ontology Definition:A Bartter disease that has_material_basis_in mutation in the MAGED2 gene on chromosome Xp11.

Synonyms: BARTS5, Bartter syndrome, type 5, antenatal, transient

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Bartter disease (is_a)