MeSH Browser

MeSH Supplementary: Iron-Refractory Iron Deficiency Anemia
Unique ID: C562385
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562385
Entry Term(s): Anemia, Hypochromic Microcytic, with Defect in Iron Metabolism; IRIDA Iron-refractory iron deficiency anemia; Iron-Handling Disorder, Hereditary; Pseudo-Iron-Deficiency Anemia
Heading Mapped to: *Anemia, Iron-Deficiency
Frequency: 74
Note: A hereditary autosomal recessive iron deficiency characterized by hypochromic microcytic anemia that is unresponsive to oral iron and only partially responsive to parenteral iron. Laboratory results show inappropriately normal or increased plasma HEPCIDIN. Mutations in the TMPRSS6 gene have been identified. OMIM: 206200
Date of Entry: 2012/11/05
Revision Date: 2019/06/18

Iron-Refractory Iron Deficiency Anemia MeSH Supplementary Concept Data 2024