237995002: Depletion of mitochondrial deoxyribonucleic acid (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Mitochondrial respiratory chain complexes disorder\Depletion of mitochondrial DNA
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Mitochondrial respiratory chain complexes disorder\Depletion of mitochondrial DNA
• \Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Mitochondrial respiratory chain complexes disorder\Depletion of mitochondrial DNA

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2970105015	Depletion of mitochondrial deoxyribonucleic acid	en	Synonym	Active	Case insensitive	SNOMED CT core
2970736019	Depletion of mitochondrial deoxyribonucleic acid (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
356709010	Depletion of mitochondrial DNA	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
626810018	Depletion of mitochondrial DNA (disorder)	en	Fully specified name	Inactive	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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