OMOP Concept 4035283
Disorder of mitochondrial respiratory chain complexes
StandardConditionSNOMED237986005Disorder
Maps from
1
Descendants
62
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Disorder of mitochondrial respiratory chain complexes via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 237986005 | Disorder of mitochondrial respiratory chain complexes | Non-standard |
Synonyms
Alternative names recorded for Disorder of mitochondrial respiratory chain complexes across source vocabularies.
- Disorder of mitochondrial respiratory chain complexes (disorder)
- Mitochondrial disorder, respiratory chain
- trastorno de los complejos de la cadena respiratoria mitocondrial
- trastorno de los complejos de la cadena respiratoria mitocondrial (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(62)Included automatically when you query with descendants.
- 13-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
- 1Acyl-CoA dehydrogenase 9 deficiency
- 1Combined oxidative phosphorylation defect type 23
- 1Combined oxidative phosphorylation defect type 26
- 1Combined oxidative phosphorylation defect type 27
- 1Combined oxidative phosphorylation defect type 29
- 1Combined oxidative phosphorylation defect type 30
- 1Deficiency in enzyme complexes of mitochondrial respiratory chain
- 1Deletion and duplication of mitochondrial DNA
- 1Depletion of mitochondrial DNA
- 1DNA2-related mitochondrial DNA deletion syndrome
- 1Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome
- 1Lethal infantile mitochondrial myopathy
- 1Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome
- 1Multiple mitochondrial dysfunctions syndrome
- 1QRSL1-related combined oxidative phosphorylation defect
- 1Severe X-linked mitochondrial encephalomyopathy
- 1Syndromic sensorineural deafness due to combined oxidative phosphorylation defect
- 2Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency
- 2Combined complex deficiencies
- 2Combined oxidative phosphorylation defect type 25
- 2Cytochrome-c oxidase deficiency
- 2Deficiency of cytochrome-b-5 reductase
- 2Deficiency of NADPH-ferrihemoprotein reductase
- 2Deficiency of NAPH cytochrome-c-2 reductase
- 2Isolated ATP synthase deficiency
- 2Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form
- 2Mitochondrial DNA depletion syndrome encephalomyopathic form
- 2Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- 2Mitochondrial DNA depletion syndrome hepatocerebrorenal form
- 2Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
- 2Multiple mitochondrial dysfunctions syndrome type 1
- 2Multiple mitochondrial dysfunctions syndrome type 2
- 2Multiple mitochondrial dysfunctions syndrome type 3
- 2Multiple mitochondrial dysfunctions syndrome type 4
- 2Multiple mitochondrial dysfunctions syndrome type 5
- 2Multiple mitochondrial dysfunctions syndrome type 6
- 2Myoclonic epilepsy myopathy sensory ataxia
- 2Navajo neurohepatopathy
- 2Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
- 2Recessive mitochondrial ataxia syndrome
- 2Succinate-coenzyme Q reductase deficiency
- 2Ubiquinone dehydrogenase deficiency
- 3Congenital lactic acidosis Saguenay-Lac-Saint-Jean type
- 3Fatal infantile cytochrome C oxidase deficiency
- 3Fatal infantile lactic acidosis with methylmalonic aciduria
- 3FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
- 3Isolated cytochrome C oxidase deficiency
- 3Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria
- 3Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
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