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
04607 CAKUTHED anomalies, congenital, kidney and urinary tract syndrome with/without hearing loss, abnormal ears, or developmental delay (CAKUTHED) 176310 - - - PBX1 - autosomal dominant
06021 CAKUTHED Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay 617641 AD 1 1 PBX1 - -
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