OMOP Concept 35622005
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
StandardConditionSNOMED763312008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 763312008 | Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome across source vocabularies.
- Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder)
- síndrome autosómico recesivo de ataxia cerebelosa, signos piramidales, nistagmo y apraxia oculomotriz
- síndrome autosómico recesivo de ataxia cerebelosa, signos piramidales, nistagmo y apraxia oculomotriz (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Amino acid transport disorder
- 1Autosomal recessive hereditary disorder
- 1Cerebellar ataxia
- 1Congenital disease
- 1Hereditary ataxia
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Cerebellar disorder
- 2Disorder of amino acid and organic acid metabolism
- 2Disorder of fetus and/or newborn
- 2Hereditary disorder of nervous system
- 2Metabolic disorder of transport
- 3Disease
- 3Disorder of amino acid metabolism
- 3Disorder of brain
- 3Disorder of nervous system
- 3Finding related to coordination / incoordination
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Metabolic disease
- 4Clinical finding
- 4Disorder of body system
- 4Disorder of head
- 4Disorder of organic acid metabolism
- 4Disorder of the central nervous system
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