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
05342 CAKUT kidney and urinary tract, anomalies, congenital (CAKUT) - - 212 212 CHRNA3, DSTYK, FOXD2, SLIT3, TBX18 - -
02984 CAKUT1;RHDNS1 kidney and urinary tract, anomalies, congenital, susceptibility to, type 1 (CAKUT-1, renal hypodysplasia, nonsyndromic, type 1 (RHDNS-1)) 610805 AD 0 0 DSTYK - -
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