1187640000: Combined oxidative phosphorylation defect type 28 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation defect type 28
• \Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation defect type 28

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4675681016	COXPD28 - combined oxidative phosphorylation defect type 28	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4675682011	Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4675685013	Combined oxidative phosphorylation defect type 28	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4675686014	Combined oxidative phosphorylation defect type 28 (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

Back to Start