720951008: Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3
• \Metabolic disease\Mitochondrial cytopathy\Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3322615013	Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3322616014	Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3322617017	Combined oxidative phosphorylation deficiency type 3	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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