About   Help   FAQ
Disease Ontology Browser
primary hypomagnesemia (DOID:0060879)
Alliance: disease page
Synonyms: HOMG; primary familial hypomagnesemia
Alt IDs: ICD10CM:E83.4, OMIM:PS602014, ORDO:34526
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.

Disease References using Mouse Models (2)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
07/02/2024
MGI 6.13 		The Jackson Laboratory