All diseases

9 entries on 1 page. Showing entries 1 - 9.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01611 DDS Denys-Drash syndrome (DDS) 194080 AD;SMu 16 16 WT1 - -
01336 Frasier Frasier syndrome 136680 AD;SMu 1 - WT1 - -
02807 Meacham Meacham syndrome 608978 - - - WT1 - -
01434 MESOM mesothelioma, malignant (MESOM) 156240 - - - BCL10, WT1 - -
00399 NPHS nephrotic syndrome (NPHS) - - 108 90 ADCK4, ARHGDIA, DAAM2, DGKE, EMP2, LAMB2, NPHS1, NPHS2, NUP205, NUP93, PLCE1, PTPRO, WT1 - -
01965 NPHS4 nephrotic syndrome, type 4 (NPHS-4) 256370 AD 2 2 WT1 - -
01610 WAGR Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome (WAGR, 11p partial monosomy syndrome) 194072 - - - PAX6, WT1 - -
00953 WAGRO Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome (WAGRO) - - - - BDNF, PAX6, WT1 - -
00774 WT1 Wilms tumor, type 1, somatic (WT-1, nephroblastoma) 194070 AD;SMu 7 7 BRCA2, GPC3, H19, WT1 - -
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