DO_rare_slim NCIthesaurus has material basis in atransferrinemia disease_ontology GARD:9595 ORDO:1195 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 (TF) on chromosome 3q22. NCI:C125693 MIM:209300 OMIM mapping confirmed by DO. [SN]. familial hypotransferrinemia autosomal recessive disease metal metabolism disorder autosomal recessive inheritance