OMOP Concept 37161015
Combined oxidative phosphorylation defect type 27
StandardConditionSNOMED1172844009Disorder
Maps from
0
Descendants
0
Valid from
30 Sept 2021
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Combined oxidative phosphorylation defect type 27 across source vocabularies.
- Combined oxidative phosphorylation defect type 27 (disorder)
- COXPD27 - combined oxidative phosphorylation defect type 27
- COXPD27 - deficiencia combinada de la fosforilación oxidativa tipo 27
- deficiencia combinada de la fosforilación oxidativa tipo 27
- deficiencia combinada de la fosforilación oxidativa tipo 27 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Degenerative brain disorder
- 1Developmental and epileptic encephalopathy
- 1Developmental hereditary disorder
- 1Disorder of mitochondrial respiratory chain complexes
- 1Hereditary degenerative disease of central nervous system
- 1Inherited metabolic disorder of nervous system
- 1Mitochondrial cytopathy
- 2Autosomal hereditary disorder
- 2Degenerative disease of the central nervous system
- 2Developmental disorder
- 2Disorder of brain
- 2Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 2Epilepsy
- 2Hereditary disease
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Metabolic disease
- 2Neurodevelopmental disorder
- 3Congenital disease
- 3Degenerative disorder
- 3Disease
- 3Disorder of head
- 3Disorder of nervous system
- 3Disorder of the central nervous system
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