763203009: Combined oxidative phosphorylation defect type 15 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation defect type 15
• \Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation defect type 15

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
3638152017	COXPD15 - combined oxidative phosphorylation defect type 15	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3638153010	Combined oxidative phosphorylation defect type 15 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3638154016	Combined oxidative phosphorylation defect type 15	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

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