736703007: Carrier of hemochromatosis HFE gene mutation (finding)

• SNOMED CT Concept\Clinical finding\...
• \General clinical state finding\Disease related state\Carrier of disorder\Carrier of haemochromatosis HFE gene mutation
• \General finding of observation of patient\General body state finding\Disease related state\Carrier of disorder\Carrier of haemochromatosis HFE gene mutation

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3521971016	Carrier of haemochromatosis HFE gene mutation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3521972011	Carrier of hemochromatosis HFE gene mutation (finding)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3521973018	Carrier of hemochromatosis HFE gene mutation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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