All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01046 CTHM heart malformations, conotruncal (CTHM) 217095 - 26 26 GATA6, GDF1, NKX2-5, NKX2-6, TBX1 - -
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