OMOP Concept 37165083
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome
StandardConditionSNOMED1237514002Disorder
Maps from
0
Descendants
0
Valid from
30 Sept 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome across source vocabularies.
- Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder)
- Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome
- síndrome de miopatía mitocondrial, ataxia cerebelosa y retinopatía pigmentaria
- síndrome de miopatía mitocondrial, ataxia cerebelosa y retinopatía pigmentaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(47)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Cerebellar ataxia
- 1Developmental delay
- 1Developmental hereditary disorder
- 1Hereditary ataxia
- 1Hereditary cerebellar atrophy
- 1Hereditary disorder of musculoskeletal system
- 1Inherited metabolic disorder of nervous system
- 1Mitochondrial myopathy
- 2Ataxia
- 2Cerebellar disorder
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary cerebellar degeneration
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Metabolic myopathy
- 2Mitochondrial cytopathy
- 3Cerebellar degeneration
- 3Congenital disease
- 3Disease
- 3Disorder of body system
- 3Disorder of brain
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