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
00522 - amyloidosis, visceral (type VIII) 105200 - - - APOA1, APOA2, B2M, FGA, LYZ - -
00538 hypoproteinemia hypoproteinemia, hypercatabolic, familial (FHH) 241600 - - - B2M - -
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