OMOP Concept 4059379
Mitochondrial myopathy
StandardConditionSNOMED16851005Disorder
Maps from
13
Descendants
44
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
13 source codes normalize to Mitochondrial myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134094 | Mitochondrial myopathy | Non-standard |
| CIM10 | G71.3 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| HPO | HP_0003737 | Mitochondrial myopathy | Non-standard |
| ICD10 | G71.3 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| ICD10CM | G71.3 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| ICD10CN | G71.3 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| ICD10CN | G71.300 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| ICD10CN | G71.301 | Mitochondrial myopathy (machine translation) | Non-standard |
| ICD10GM | G71.3 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| KCD7 | G71.3 | Mitochondrial myopathy, NEC | Non-standard |
| MeSH | D017240 | Mitochondrial Myopathies | Non-standard |
| Read | F39X.00 | Mitochondrial myopathy, not elsewhere classified | Non-standard |
| Read | Fyu8A00 | [X]Mitochondrial myopathy, not elsewhere classified | Non-standard |
Synonyms
Alternative names recorded for Mitochondrial myopathy across source vocabularies.
- miopatía mitocondrial
- miopatía mitocondrial (trastorno)
- Mitochondrial myopathy (disorder)
- Ragged red myopathy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
Narrower concepts
(44)Included automatically when you query with descendants.
- 1Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
- 1Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency
- 1Autosomal dominant mitochondrial myopathy with exercise intolerance
- 1Childhood-onset spasticity with hyperglycinemia
- 1Combined oxidative phosphorylation defect type 39
- 1Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- 1Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
- 1DNA2-related mitochondrial DNA deletion syndrome
- 1Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- 1Juvenile myopathy AND lactate acidosis
- 1Lethal infantile mitochondrial myopathy
- 1Luft's hypermetabolic myopathy
- 1Maternally inherited mitochondrial cardiomyopathy and myopathy
- 1Maternally inherited mitochondrial myopathy
- 1Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form
- 1Mitochondrial encephalomyopathy
- 1Mitochondrial-lipid-glycogen storage myopathy
- 1Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome
- 1Mitochondrial myopathy, lactic acidosis, deafness syndrome
- 1Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
- 1Mitochondrial myopathy with sideroblastic anemia syndrome
- 1Myopathy and diabetes mellitus
- 1Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
- 1Periodic paralysis with later-onset distal motor neuropathy
- 1Progressive external ophthalmoplegia, myopathy, emaciation syndrome
Showing 25 of 44. Retrieve the full set via the API.
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