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 - -
00176 HDLCD-2 hypoalphalipoproteinemia (HDL deficiency, type 2 (HDLCD-2)) 604091 - - - ABCA1, APOA1 - -
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