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
00104 EHT hypertension, essential, susceptibility to (EHT) 145500 Mu 2 388 ADD1, AGT, AGTR1, ATP1B1, CYP3A5, ECE1, GNB3, NOS2, NOS3, PTGIS, RGS5, SELE - -
03475 HCAD Hirschsprung disease, cardiac defects, autonomic dysfunction (HCAD) 613870 AD 7 - ECE1 - -
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