All diseases

4 entries on 1 page. Showing entries 1 - 4.
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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 AD 3 2 APOA1, APOA2, B2M, FGA, LYZ - -
00174 FH hypercholesterolemia, familial (FH) - AD 2962 2944 ABCA1, APOA2, EPHX2, GHR, ITIH4, LDLR, PPP1R17 - -
05708 FHCL1 hypercholesterolemia, familial, type 1 (FHCL1) 143890 AD 1 1 APOA2, EPHX2, GHR, LDLR - -
00523 renal failure renal failure - - 4 4 APOA2 - -
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