Disorders


 

Hypochromic Microcytic Anemia with Iron Overload


 

OMIM

GeneLocusProtein
SLC11A212q13Natural resistance-associated macrophage protein 2

Laboratory Test Method Prenatal Carrier *
Institute of Predictive and Personalized Medicine of Cancer, Advanced Genetic Diagnostic Unit for Rare Iron Metabolism Disorders (UDGAEMH) - Barcelona, Spain  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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