766929007: Genetic hyperferritinemia without iron overload (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level\Finding of blood substance level\Blood substance level above reference range\Serum ferritin above reference range\Genetic hyperferritinemia without iron overload
• \Finding of substance level\Protein level - finding\Serum ferritin above reference range\Genetic hyperferritinemia without iron overload
• \Measurement finding outside reference range\Measurement finding above reference range\Blood substance level above reference range\Serum ferritin above reference range\Genetic hyperferritinemia without iron overload
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Genetic hyperferritinemia without iron overload

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3663200016	Genetic hyperferritinemia without iron overload	en	Synonym	Active	Case insensitive	SNOMED CT core
3663201017	Benign hyperferritinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3663202012	Genetic hyperferritinemia without iron overload (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3663203019	A rare biological anomaly defined as high serum ferritin levels without elevations of transferrin saturation, tissue or serum iron and with characteristics of an apparently asymptomatic clinical phenotype.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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