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
00399 NPHS nephrotic syndrome (NPHS) - - 30 28 ADCK4, ARHGDIA, DGKE, EMP2, LAMB2, NPHS1, NPHS2, NUP205, NUP93, PLCE1, PTPRO, WT1 - -
05447 NPHS-12 nephrotic syndrome, type 12 (NPHS-12) 616892 - 0 0 NUP93 - autosomal recessive
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