Human genes for atransferrinemia
Atransferrinemia [DOID:0050649]
A metal metabolism disorder that is characterized by transferrin deficiency, microcytic anemia, and iron loading, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the structural gene for transferrin on chromosome 3q22.
Synonyms: atransferrinemia, atransferrinemias, DOID:0050649, familial hypotransferrinemia, hereditary hypotransferrinemia ...
Linkouts: OMIM