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
03346 CDG2J glycosylation, congenital disorder of, type IIj (CDG-2J) 613489 AR - - COG4 - -
05492 SWILS Saul-Wilson syndrome (SWILS) 618150 AD 14 14 COG4 - autosomal dominant
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