All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00457 - afibrinogenemia, congenital 202400 3 3 FGA, FGB, FGG - -
04471 - Dysfibrinogenemia, congenital 616004 0 0 FGA, FGB, FGG - -