763110007: Combined oxidative phosphorylation defect type 13 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation defect type 13
• \Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation defect type 13

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3637892016	Combined oxidative phosphorylation defect type 13 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3637893014	Combined oxidative phosphorylation defect type 13	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3637894015	COXPD13 - combined oxidative phosphorylation defect type 13	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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