402788005: Genetic disorder of lipid storage (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipid storage disease\Genetic disorder of lipid storage
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipid storage disease\Genetic disorder of lipid storage
• \Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Lipid storage disease\Genetic disorder of lipid storage
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Lipid storage disease\Genetic disorder of lipid storage
• \Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipid storage disease\Genetic disorder of lipid storage

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1770712018	Genetic disorder of lipid storage (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
1781880010	Genetic disorder of lipid storage	en	Synonym	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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