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
03648 ARCL1B cutis laxa, autosomal recessive, type 1B (ARCL-1B) 614437 AR 1 1 EFEMP2 - -
00399 NPHS nephrotic syndrome (NPHS) - - 108 90 ADCK4, ARHGDIA, DAAM2, DGKE, EMP2, LAMB2, NPHS1, NPHS2, NUP205, NUP93, PLCE1, PTPRO, WT1 - -
04109 NPHS10 nephrotic syndrome, type 10 615861 AR - - EMP2 - -
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