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DOID:0060885 - renal hypomagnesemia 2
Disease Ontology 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.
Synonyms: HOMG2, autosomal dominant primary hypomagnesemia with hypocalciuria,
Xenbase Genes
:
fxyd2,
hnf1b
| MONDO:0007937 - renal hypomagnesemia 2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary hypomagnesemia (is_a)