1187514002: Myopathic form of carnitine palmitoyltransferase II deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\...
• \Fatty acid oxidation defect\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Carnitine palmitoyltransferase deficiency\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatty acid oxidation defect\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of fatty acid metabolism\Carnitine palmitoyltransferase deficiency\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Organic acid metabolism disorder\Disorder of fatty acid metabolism\Carnitine palmitoyltransferase deficiency\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Enzymopathy\Carnitine palmitoyltransferase deficiency\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Fatty acid oxidation defect\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of fatty acid metabolism\Carnitine palmitoyltransferase deficiency\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of fatty acid metabolism\...
• \Fatty acid oxidation defect\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency
• \Carnitine palmitoyltransferase deficiency\Carnitine palmitoyltransferase II deficiency\Myopathic form of carnitine palmitoyltransferase II deficiency

Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4674057017	Myopathic form of carnitine palmitoyltransferase II deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
4674058010	Myopathic form of carnitine palmitoyltransferase II deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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