724279004: Combined oxidative phosphorylation defect type 5 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation defect type 5
• \Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation defect type 5

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3433539014	Combined oxidative phosphorylation defect type 5 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3433540011	Combined oxidative phosphorylation defect type 5	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3433541010	COXPD5 - combined oxidative phosphorylation defect 5	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3433542015	Hypotonia with lactic acidemia and hyperammonemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3433543013	Hypotonia with lactic acidaemia and hyperammonaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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