All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03730 - CFHR5 deficiency 614809 AD - - CFHR5 - -
01838 AHUS1 hemolytic-uremic syndrome, atypical, type 1 (AHUS1) 235400 AD;AR - - CFH, CFHR1, CFHR3 - -
00347 ARMD macular degeneration, age-related (ARMD) - - 30 34 ABCA4, CFH, FBLN5, HMCN1 - -
00395 ARMD1 macular degeneration, age-related, type 1 (ARMD-1) 603075 AD - - APOE, CFHR1, CFHR3, HMCN1, PLEKHA1 - -
00348 ARMD4 macular degeneration, age-related, type 4 (ARMD-4) 610698 - - - CFH - -
00346 BLD basal laminar drusen (BLD) 126700 AD - - CFH - -
00345 CFHD deficiency, complement factor H (CFHD) 609814 AD;AR - - CFH - -
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