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