766876004: Combined oxidative phosphorylation defect type 4 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation defect type 4
• \Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation defect type 4

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
3662982014	Combined oxidative phosphorylation defect type 4	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3662983016	COXPD4 - combined oxidative phosphorylation defect type 4	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3662984010	Combined oxidative phosphorylation defect type 4 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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