All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03482 HOMG6 hypomagnesemia, type 6, renal (HOMG-6) 613882 AD - - CNNM2 - -
04417 HOMGSMR hypomagnesemia, seizures, and mental retardation (HOMGSMR) 616418 AD;AR - - CNNM2 - -
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