766929007: hyperferritinémie génétique sans surcharge en fer (trouble)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Protein level - finding\Serum ferritin high (finding)\Genetic hyperferritinemia without iron overload

\Measurement finding outside reference range\Measurement finding above reference range\Serum ferritin high (finding)\Genetic hyperferritinemia without iron overload

\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Genetic hyperferritinemia without iron overload

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1015211000172111 hyperferritinémie bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3663200016 Genetic hyperferritinemia without iron overload en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3663201017 Benign hyperferritinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3663202012 Genetic hyperferritinemia without iron overload (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

768601000241112 hyperferritinémie génétique sans surcharge en fer (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

988321000172114 hyperferritinémie génétique sans surcharge en fer fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

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 Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Genetic hyperferritinemia without iron overload	est un(e) (attribut)	Serum ferritin high (finding)	true	Inferred relationship	Some
Genetic hyperferritinemia without iron overload	a pour interprétation (attribut)	au-dessus de l'étendue de référence	true	Inferred relationship	Some	1
Genetic hyperferritinemia without iron overload	interprète (attribut)	Serum ferritin measurement	true	Inferred relationship	Some	1
Genetic hyperferritinemia without iron overload	est un(e) (attribut)	Autosomal hereditary disorder	true	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets