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DOID:0060879 - primary hypomagnesemia
Disease Ontology Definition:A metal metabolism disorder characterized by very low serum magnesium levels often with secondary hypocalcemia with onset typically in the first months of life.
Synonyms: HOMG, primary familial hypomagnesemia,
Xenbase Genes
:
fxyd2,
hnf1b,
egf,
cldn19,
trpm6,
cldn16,
cnnm2
| MONDO:0018100 - familial primary hypomagnesemia |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
metal metabolism disorder (is_a)