TFR2

transferrin receptor 2
OMIM: 604720
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 2.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hemochromatosis, type 3 604250, Hereditary haemochromatosis Type 3 (Disorder of iron metabolism)
R-numbers: R96
Signed-off version 1.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
604250 HEMOCHROMATOSIS, TYPE 3, 604250 Hemochromatosis, type 3, HFE3