All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03078 CDG-1N glycosylation, congenital disorder of, type In (CDG-1N) 612015 0 0 RFT1 - -