OMOP Concept 36715138
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
StandardConditionSNOMED720634003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535351 | CAPOS syndrome | Non-standard |
Synonyms
Alternative names recorded for Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome across source vocabularies.
- CAPOS (cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss) syndrome
- Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (disorder)
- síndrome de ataxia cerebelosa, arreflexia, pie cavo, atrofia óptica, hipoacusia neurosensorial
- síndrome de ataxia cerebelosa, arreflexia, pie cavo, atrofia óptica, hipoacusia neurosensorial (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(52)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Disorder of ear
- 1Early onset cerebellar ataxia
- 1Hearing loss associated with syndrome
- 1Hereditary ataxia
- 1Hereditary hearing loss
- 1Inherited optic neuropathy
- 1Multiple system malformation syndrome
- 2Ataxia
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Cerebellar ataxia
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of head
- 2Disorder of optic nerve
- 2Disorder of sensory organ
- 2Ear finding
- 2Ear, nose and throat disorder
- 2Hearing loss
- 2Hereditary disease
- 2Hereditary disorder of nervous system
- 2Hereditary disorder of the visual system
Showing 25 of 52. Retrieve the full set via the API.
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