237994003: Deletion and duplication 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\Deletion and duplication 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\Deletion and duplication of mitochondrial DNA
• \Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Mitochondrial respiratory chain complexes disorder\Deletion and duplication of mitochondrial DNA

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2970493013	Deletion and duplication of mitochondrial deoxyribonucleic acid	en	Synonym	Active	Case insensitive	SNOMED CT core
2970556016	Deletion and duplication of mitochondrial deoxyribonucleic acid (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
356708019	Deletion and duplication of mitochondrial DNA	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
626809011	Deletion and duplication 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

Description inactivation indicator reference set

REPLACED BY association reference set

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