OMOP Concept 4043571
Congenital nuclear ophthalmoplegia
StandardConditionSNOMED230530003Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital nuclear ophthalmoplegia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 230530003 | Congenital nuclear ophthalmoplegia | Non-standard |
Synonyms
Alternative names recorded for Congenital nuclear ophthalmoplegia across source vocabularies.
- Congenital nuclear ophthalmoplegia (disorder)
- oftalmoplejía nuclear congénita
- oftalmoplejía nuclear congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(44)Roll up to these when you need a wider cohort.
- 1Congenital structural abnormality of eyelid
- 1Disorder of midbrain
- 1Dysgenesis of the brainstem
- 1Ophthalmoplegia
- 2Congenital anomaly of brain
- 2Congenital anomaly of face
- 2Congenital anomaly of ocular adnexa
- 2Disorder of brain stem
- 2Disorder of eyelid
- 2Neurologic disorder of eye movements
- 2Paralytic syndrome
- 3Congenital anomaly of central nervous system
- 3Congenital anomaly of head
- 3Congenital anomaly of visual system
- 3Disorder of brain
- 3Disorder of eye movements
- 3Disorder of face
- 3Disorder of nervous system
- 3Disorder of ocular adnexa
- 3Eyelid finding
- 3Movement disorder
- 3Paralysis
- 4Congenital anomaly of nervous system
- 4Congenital malformation
- 4Disease
Narrower concepts
(1)Included automatically when you query with descendants.
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