Bartter disease type 5

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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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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

Parent(s): Bartter disease (is_a)