All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03467 CHTD6 heart defects, congenital, multiple types, type 6 (CHTD-6) 613854 AD - - GDF1 - -
01046 CTHM heart malformations, conotruncal (CTHM) 217095 - 26 26 GATA6, GDF1, NKX2-5, NKX2-6, TBX1 - -
01668 RAI atrial isomerism, right (RAI) 208530 AR 2 2 GDF1 - -
00389 TOF tetralogy of Fallot (TOF) 187500 AD 102 94 GATA4, GATA6, GDF1, JAG1, NKX2-5, TBX1, ZFPM2 - -
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