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
05342 CAKUT kidney and urinary tract, anomalies, congenital (CAKUT) - - 212 212 CHRNA3, DSTYK, FOXD2, SLIT3, TBX18 - -
05341 CAKUT2 kidney and urinary tract, anomalies, congenital, type 2 (CAKUT-2) 143400 AD - - TBX18 - -
01371 HD Huntington disease (HD) 143100 AD 65 65 HTT, TBX18 - -
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