82500001: Wolman's disease (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Lysosomal acid lipase deficiency\Wolman's disease
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Lysosomal acid lipase deficiency\Wolman's disease
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Lysosomal acid lipase deficiency\Wolman's disease
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Lysosomal acid lipase deficiency\Wolman's disease
• \Congenital disease\Inborn error of metabolism\Lysosomal acid lipase deficiency\Wolman's disease

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
136837016	Wolman's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
136838014	Primary familial xanthomatosis with adrenal calcification	en	Synonym	Active	Case insensitive	SNOMED CT core
136839018	Familial visceral xanthomatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
136843019	Deficiency of cholesterol esterase AND triacylglycerol lipase	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
201017015	Wolman xanthomatosis	en	Synonym	Active	Case sensitive	SNOMED CT core
201018013	Primary familial xanthomatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
505109013	Wolman disease	en	Synonym	Active	Case sensitive	SNOMED CT core
505110015	Acid esterase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
505111016	Acid lipase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
823935018	Wolman's disease (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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