OMOP Concept 36713765
X-linked cone dysfunction syndrome with myopia
StandardConditionSNOMED718718009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to X-linked cone dysfunction syndrome with myopia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564092 | Bornholm Eye Disease | Non-standard |
| Nebraska Lexicon | 718718009 | X-linked cone dysfunction syndrome with myopia | Non-standard |
Synonyms
Alternative names recorded for X-linked cone dysfunction syndrome with myopia across source vocabularies.
- Bornholm eye disease
- síndrome de disfunción de conos con miopía ligado al cromosoma X
- síndrome de disfunción de conos con miopía ligado al cromosoma X (trastorno)
- síndrome ocular de Bornholm
- X-linked cone dysfunction syndrome with myopia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Hereditary disorder of the visual system
- 1Myopia
- 1X-linked recessive hereditary disease
- 2Disorder of refraction
- 2Hereditary disorder by system
- 2Visual system disorder
- 2X-linked hereditary disease
- 3Disorder of body system
- 3Disorder of refraction AND/OR accommodation
- 3Eye / vision finding
- 3Hereditary disease
- 3Sex-linked hereditary disorder
- 4Clinical finding
- 4Disease
- 4Disorder of vision
- 4Genetic disease
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