EPHX2

epoxide hydrolase 2
OMIM: 132811, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red EPHX2 in Familial hypercholesterolaemia

Level 3: Arteriopathies
Level 2: Cardiovascular disorders
Version 1.27

review Not set
Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Hypercholesterolemia, familial, due to LDLR defect, modifier of, 143890