All diseases

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00557 - Cousin syndrome 260660 - - - TBX15 - -
01047 - DiGeorge syndrome 188400 - - - TBX1 - -
01048 - velocardiofacial syndrome 192430 - - - DGCR14, DGCR2, DGCR6, DGCR8, TBX1 - -
01623 - ACTH deficiency 201400 - - - TBX19 - -
01046 CTHM heart malformations,conotruncal (CTHM) 217095 - - - CFC1, GATA6, GDF1, NKX2-5, NKX2-6, TBX1 - -
01371 HD Huntington disease (HD) 143100 - - - HTT, TBX18 - -
00389 TOF tetralogy of Fallot (TOF) 187500 - - - GATA4, GATA6, GDF1, JAG1, NKX2-5, TBX1, ZFPM2 - -
Legend   How to query