OMOP Concept 37161014
Combined oxidative phosphorylation defect type 29
StandardConditionSNOMED1172843003Disorder
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 29 across source vocabularies.
- Combined oxidative phosphorylation defect type 29 (disorder)
- COXPD29 - combined oxidative phosphorylation defect type 29
- COXPD29 - deficiencia combinada de la fosforilación oxidativa tipo 29
- deficiencia combinada de la fosforilación oxidativa tipo 29
- deficiencia combinada de la fosforilación oxidativa tipo 29 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of mitochondrial respiratory chain complexes
- 1Hereditary cerebellar atrophy
- 1Inherited metabolic disorder of nervous system
- 1Mitochondrial cytopathy
- 2Autosomal hereditary disorder
- 2Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 2Hereditary cerebellar degeneration
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Metabolic disease
- 3Cerebellar degeneration
- 3Congenital disease
- 3Disease
- 3Disorder of nervous system
- 3Hereditary degenerative disease of central nervous system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 4Cerebellar disorder
- 4Clinical finding
- 4Degenerative brain disorder
- 4Degenerative disease of the central nervous system
- 4Disorder of body system
- 4Fetal and/or neonatal disorder
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