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
03475 - Hirschsprung disease, cardiac defects, and autonomic dysfunction 613870 - - - ECE1 - -
00104 EHT hypertension, essential (EHT) 145500 - - - ADD1, AGT, AGTR1, ATP1B1, CYP3A5, ECE1, GNB3, NOS2, NOS3, PTGIS, RGS5, SELE - -
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