Orphanet: Molecular diagnosis of hemochromatosis HFE, HFE2, HAMP, TFR2 and SLC40A1 genes

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Molecular diagnosis of hemochromatosis (HFE, HFE2, HAMP, TFR2 and SLC40A1 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 25/09/2015
  • Genome Center of Eastern Finland
  • University of Eastern Finland
  • Yliopistonranta 1
  • 70210 KUOPIO
  • Director of laboratory : Pr Markku LAAKSO
  • More information
  • Phone : -
  • Additional Phone : -
  • Fax : -
  • Website
  • Contact
Last update: September 2015

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
NGS sequencing (except WES)

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (5)

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.