698290008: X-linked creatine deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked creatine deficiency
• \Metabolic disease\Metabolic disorder of transport\X-linked creatine deficiency

Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2973816011	X-linked creatine deficiency syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2973817019	SLC6A8 related creatine transporter deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
2973820010	X-linked creatine deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
2973824018	Creatine transporter deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
2973826016	X-linked creatine deficiency (disorder)	en	Fully specified name	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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