238067002: Peroxisomal thiolase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Peroxisomal thiolase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Peroxisomal thiolase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Peroxisomal thiolase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356849011	Peroxisomal thiolase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
356850011	Pseudo-Zellweger syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
356851010	3-Ketoacyl-CoA thiolase deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
626899016	Peroxisomal thiolase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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