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
01838 AHUS1 hemolytic-uremic syndrome, atypical, type 1 (AHUS1) 235400 AD;AR - - CFH, CFHR1, CFHR3 - -
00395 ARMD1 macular degeneration, age-related, type 1 (ARMD-1) 603075 AD - - APOE, CFHR1, CFHR3, HMCN1, PLEKHA1 - -
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