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Genetic hyperferritinemia without iron overload
Disease definition
Genetic hyperferritinemia without iron overload is a rare biological anomaly defined as high serum ferritin levels without elevations of transferrin saturation, tissue or serum iron and characterized by an apparently asymptomatic clinical phenotype.
ORPHA:254704
Classification level: Disorder- Synonym(s):
- Benign hyperferritinemia
- Prevalence: Unknown
- Inheritance: Autosomal recessive or Autosomal dominant
- Age of onset: No data available
- ICD-10: R77.8
- OMIM: -
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
A summary on this disease is available in Deutsch (2018) Español (2018) Italiano (2018) Nederlands (2018)
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