All diseases

2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00399 NPHS nephrotic syndrome (NPHS) - 15 13 EMP2, NPHS1 - -
00074 NPHS-1 nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF)) 256300 3 3 NPHS1 - -