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Standards Ontologies Notations
primary hypomagnesemia

Summary
Synonym
  • HOMG
  • primary familial hypomagnesemia
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.
Super Class
metal metabolism disorder
Disease Ontology
DOID:0060879
ORDO
OMIM
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1950 EGF epidermal growth factor
55644 OSGEP O-sialoglycoprotein endopeptidase
Displaying 1 entry
Gene ID Gene Symbol Description Source
13645 Egf epidermal growth factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
25313 Egf epidermal growth factor
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024