Disorders

Iron Overload, Autosomal Dominant

Gene	Locus	Protein
FTH1	11q13	Ferritin heavy chain

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	• Sequence analysis of the entire coding region

^* 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.