All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02199 CDG2M glycosylation, congenital disorder of, type IIm (CDG-2M) 300896 SMo;XLD 28 - SLC35A2 - -
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