"ORDO:1195"^^ . . "disease_ontology"^^ . "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."^^ . _:vb50937325 . "DOID:0050649"^^ . "NCI:C125693"^^ . "GARD:9595"^^ . "OMIM:209300"^^ . _:vb50937325 . _:vb50937325 . _:vb50937325 . "atransferrinemia"^^ . . _:vb50937325 . "OMIM mapping confirmed by DO. [SN]."^^ . . . "familial hypotransferrinemia"@en . .