783178001: Combined oxidative phosphorylation deficiency type 20 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation deficiency type 20
• \Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation deficiency type 20

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3757969012	Combined oxidative phosphorylation deficiency type 20 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3757970013	Combined oxidative phosphorylation deficiency type 20	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3757971012	COXPD20 - combined oxidative phosphorylation deficiency type 20	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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