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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356849011	Peroxisomal thiolase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
356850011	Pseudo-Zellweger syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356851010	3-Ketoacyl-CoA thiolase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
626899016	Peroxisomal thiolase deficiency (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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