renal hypomagnesemia 2 Disease Ontology Browser

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renal hypomagnesemia 2 (DOID:0060885)
Alliance: disease page
Synonyms: autosomal dominant primary hypomagnesemia with hypocalciuria; HOMG2
Alt IDs: OMIM:154020, ICD10CM:E83.4, ORDO:34528
Definition: A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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