EGLN3

egl-9 family hypoxia inducible factor 3
OMIM: 606426, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red EGLN3 in Hereditary Erythrocytosis

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 2.6
Latest signed off version: v2.0 (22 Mar 2023)

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Familial erythrocytosis