703388005: Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\GRACILE syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3008403015	Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death	en	Synonym	Active	Case insensitive	SNOMED CT core
3008466014	Fellman syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3008482010	Finnish lethal neonatal metabolic syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3008518016	GRACILE syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3008540013	Finnish lactic acidosis with hepatic hemosiderosis	en	Synonym	Active	Case sensitive	SNOMED CT core
3008547011	Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death (disorder)	en	Fully specified name	Active	Case insensitive	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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