All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01188 ASD7 septal defect, atrial, type 7 with/without atrioventricular conduction defects (ASD7) 108900 AD 74 74 NKX2-5 - -
01766 CHNG5 hypothyroidism, congenital, nongoitrous, type 5 (CHNG5) 225250 AD 33 33 NKX2-5 - -
01046 CTHM heart malformations, conotruncal (CTHM) 217095 - 26 26 GATA6, GDF1, NKX2-5, NKX2-6, TBX1 - -
00140 HLHS2 heart, hypoplastic left, syndrome, type 2 (HLHS-2) 614435 AD 2 1 NKX2-5 - -
00389 TOF tetralogy of Fallot (TOF) 187500 AD 102 94 GATA4, GATA6, GDF1, JAG1, NKX2-5, TBX1, ZFPM2 - -
03644 VSD3 septal, ventricular defect, type 3 (VSD-3) 614432 AD - - NKX2-5 - -
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