784370005: Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Musculoskeletal finding\Disorder of musculoskeletal system\...
• \Hereditary disorder of musculoskeletal system\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Disorder of mitochondrial respiratory chain complexes\Deficiency in enzyme complexes of mitochondrial respiratory chain\Cytochrome-c oxidase deficiency\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Disorder of mitochondrial respiratory chain complexes\Deficiency in enzyme complexes of mitochondrial respiratory chain\Cytochrome-c oxidase deficiency\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Metabolic disease\Mitochondrial cytopathy\Cytochrome-c oxidase deficiency\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Metabolic disease\Mitochondrial cytopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Metabolic disease\Enzymopathy\Deficiency in enzyme complexes of mitochondrial respiratory chain\Cytochrome-c oxidase deficiency\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Disorder of mitochondrial respiratory chain complexes\Deficiency in enzyme complexes of mitochondrial respiratory chain\Cytochrome-c oxidase deficiency\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Mitochondrial myopathy\Mitochondrial myopathy with reversible cytochrome C oxidase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3763821014	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3763822019	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3763823012	Benign COX (cytochrome C oxidase) deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3763824018	Mitochondrial myopathy with reversible complex IV deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3763825017	Reversible infantile cytochrome C oxidase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3763826016	Infantile reversible cytochrome C oxidase deficiency myopathy	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3763827013	Reversible infantile respiratory chain deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3763828015	Mitochondrial myopathy with reversible COX (cytochrome C oxidase) deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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