U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Isolated hyperferritinemia

Summary

Hyperferritinemia (HRFT) is an autosomal recessive condition characterized by increased serum ferritin levels in the absence of iron overload or other clinical symptoms (Monfrini et al., 2023). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: CLEVER-1, FEEL-1, FEEL1, FELE-1, FEX1, HRFT, SCARH2, STAB-1, STAB1
    Summary: stabilin 1

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.