All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04606 FSGS-7 glomerulosclerosis, focal segmental, type 7 (FSGS-7) 616002 - - - PAX2 - -
01257 PAPRS papillorenal syndrome (PAPRS, renal coloboma syndrome) (PAPRS) 120330 - - - PAX2 - -
01593 RHDA-1 hypodysplasia/aplasia, renal, type 1 (RHDA-1) 191830 - - - ITGA8, PAX2, RET - -
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