DISEASES

Disease-gene associations mined from literature

Human genes for hemochromatosis type 3

Hemochromatosis type 3 [DOID:0111030]

A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22.

Synonyms:  hemochromatosis type 3,  DOID:0111030,  hemochromatosis due to defect in transferrin receptor 2,  HFE3,  TFR2-related hemochromatosis ...