OMOP Concept 44782474
Myoclonic epilepsy myopathy sensory ataxia
StandardConditionSNOMED699328003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Myoclonic epilepsy myopathy sensory ataxia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564395 | Spinocerebellar Ataxia with Epilepsy | Non-standard |
Synonyms
Alternative names recorded for Myoclonic epilepsy myopathy sensory ataxia across source vocabularies.
- MEMSA - myoclonic epilepsy myopathy sensory ataxia
- Myoclonic epilepsy myopathy sensory ataxia (disorder)
- síndrome epilepsia mioclónica, miopatía y ataxia sensitiva
- síndrome epilepsia mioclónica, miopatía y ataxia sensitiva (trastorno)
- Spinocerebellar ataxia with epilepsy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Depletion of mitochondrial DNA
- 1Hereditary cerebellar degeneration
- 1Inherited metabolic disorder of nervous system
- 1Spinocerebellar disease
- 2Autosomal hereditary disorder
- 2Cerebellar degeneration
- 2Cerebellar disorder
- 2Disorder of mitochondrial respiratory chain complexes
- 2Encephalomyelopathy
- 2Hereditary degenerative disease of central nervous system
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 3Congenital disease
- 3Degenerative brain disorder
- 3Degenerative disease of the central nervous system
- 3Disorder of brain
- 3Disorder of nervous system
- 3Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 3Spinal cord disease
- 4Degenerative disorder
- 4Disorder of body system
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