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DOID:0060884 - renal hypomagnesemia 6
Disease Ontology Definition:A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24.
Synonyms: HOMG6,
Xenbase Genes
:
cnnm2
| MONDO:0013480 - renal hypomagnesemia 6 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary hypomagnesemia (is_a)