All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00457 - afibrinogenemia, congenital 202400 AR 3 3 FGA, FGB, FGG - -
00522 - amyloidosis, visceral (type VIII) 105200 AD 3 2 APOA1, APOA2, B2M, FGA, LYZ - -
04471 - Dysfibrinogenemia, congenital 616004 - 1 1 FGA, FGB, FGG - -
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