DISEASES

Disease-gene associations mined from literature

Human genes for hemochromatosis type 1

Hemochromatosis type 1 [DOID:0111029]

A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22.

Synonyms:  hemochromatosis type 1,  DOID:0111029,  HFE1,  symptomatic form of HFE-related hereditary hemochromatosis,  symptomatic form of classic hemochromatosis ...