OMOP Concept 81539
Mitochondrial cytopathy
StandardConditionSNOMED240096000Disorder
Maps from
6
Descendants
125
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Mitochondrial cytopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134095 | Mitochondrial cytopathy | Non-standard |
| ICD10GM | G31.81 | Mitochondrial cytopathy | Non-standard |
| ICD9CM | 277.87 | Disorders of mitochondrial metabolism | Non-standard |
| MeSH | C540770 | Mitochondrial cytopathy | Non-standard |
| MeSH | D028361 | Mitochondrial Diseases | Non-standard |
| Nebraska Lexicon | 240096000 | Mitochondrial cytopathy | Non-standard |
Synonyms
Alternative names recorded for Mitochondrial cytopathy across source vocabularies.
- citopatía mitocondrial
- citopatía mitocondrial (trastorno)
- Mitochondrial cytopathy (disorder)
- Mitochondrial disease
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(125)Included automatically when you query with descendants.
- 1Auditory neuropathy, optic atrophy syndrome
- 1Autosomal dominant optic atrophy plus syndrome
- 1Autosomal dominant progressive external ophthalmoplegia
- 1Autosomal recessive ataxia due to ubiquinone deficiency
- 1Autosomal recessive optic atrophy type 7
- 1Autosomal recessive progressive external ophthalmoplegia
- 1Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
- 1Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
- 1Childhood myocerebrohepatopathy spectrum
- 1Chronic diarrhea with villous atrophy syndrome
- 1Combined oxidative phosphorylation defect type 11
- 1Combined oxidative phosphorylation defect type 13
- 1Combined oxidative phosphorylation defect type 14
- 1Combined oxidative phosphorylation defect type 15
- 1Combined oxidative phosphorylation defect type 17
- 1Combined oxidative phosphorylation defect type 2
- 1Combined oxidative phosphorylation defect type 21
- 1Combined oxidative phosphorylation defect type 23
- 1Combined oxidative phosphorylation defect type 24
- 1Combined oxidative phosphorylation defect type 25
- 1Combined oxidative phosphorylation defect type 26
- 1Combined oxidative phosphorylation defect type 27
- 1Combined oxidative phosphorylation defect type 28
- 1Combined oxidative phosphorylation defect type 29
- 1Combined oxidative phosphorylation defect type 30
- 1Combined oxidative phosphorylation defect type 4
- 1Combined oxidative phosphorylation defect type 5
- 1Combined oxidative phosphorylation defect type 7
- 1Combined oxidative phosphorylation defect type 8
- 1Combined oxidative phosphorylation defect type 9
- 1Combined oxidative phosphorylation deficiency type 20
- 1Cytochrome-c oxidase deficiency
- 1Deficiency of mitochondrial complex III
- 1Demyelination of central nervous system co-occurrent and due to mitochondrial disease
- 1Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- 1Encephalopathy due to mitochondrial and peroxisomal fission defect
- 1Epileptic encephalopathy with global cerebral demyelination
- 1Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3
- 1Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
- 1Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome
- 1Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- 1Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- 1Infantile onset spinocerebellar ataxia
- 1Kearns-Sayre syndrome
- 1Leber's optic atrophy
- 1Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome
- 1Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome
- 1Lipoic acid synthetase deficiency
- 1Lipoyl transferase 1 deficiency
- 1Liver disease co-occurrent and due to mitochondrial disorder
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