1172841001: Combined oxidative phosphorylation defect type 30 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Combined oxidative phosphorylation defect type 30
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Combined oxidative phosphorylation defect type 30
• \Musculoskeletal finding\Musculoskeletal disorder\...
• \Hereditary disorder of musculoskeletal system\Combined oxidative phosphorylation defect type 30
• \Disorder of skeletal muscle\Combined oxidative phosphorylation defect type 30
• \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\Combined oxidative phosphorylation defect type 30
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Combined oxidative phosphorylation defect type 30
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Combined oxidative phosphorylation defect type 30
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Combined oxidative phosphorylation defect type 30
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined oxidative phosphorylation defect type 30
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Combined oxidative phosphorylation defect type 30
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Combined oxidative phosphorylation defect type 30
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Combined oxidative phosphorylation defect type 30
• \Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Combined oxidative phosphorylation defect type 30
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Combined oxidative phosphorylation defect type 30
• \Disease\Myopathy\Disorder of skeletal muscle\Combined oxidative phosphorylation defect type 30
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Mitochondrial respiratory chain complexes disorder\Combined oxidative phosphorylation defect type 30
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Combined oxidative phosphorylation defect type 30
• \Disease\Metabolic disease\Mitochondrial cytopathy\Combined oxidative phosphorylation defect type 30
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Mitochondrial respiratory chain complexes disorder\Combined oxidative phosphorylation defect type 30
• \Disease\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Combined oxidative phosphorylation defect type 30
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Combined oxidative phosphorylation defect type 30

Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4636164010	Combined oxidative phosphorylation defect type 30	en	Synonym	Active	Case insensitive	SNOMED CT core
4636165011	Combined oxidative phosphorylation defect type 30 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4636166012	COXPD30 - combined oxidative phosphorylation defect type 30	en	Synonym	Active	Case sensitive	SNOMED CT core
4636167015	A rare mitochondrial oxidative phosphorylation disorder with characteristics of neonatal onset of hypotonia, feeding difficulties, deafness, and early fatal respiratory failure. Cardiac and liver involvement has been reported. Serum lactate is increased and metabolic studies show decreased activity of mitochondrial respiratory complexes I and IV in skeletal muscle.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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