OMOP Concept 4304093
Schnyder crystalline cornea dystrophy
StandardConditionSNOMED419395007Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2006
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Schnyder crystalline cornea dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143107 | Crystalline corneal dystrophy | Non-standard |
| MeSH | C535475 | Corneal Dystrophy, Crystalline, of Schnyder | Non-standard |
| Nebraska Lexicon | 419395007 | Schnyder crystalline cornea dystrophy | Non-standard |
Synonyms
Alternative names recorded for Schnyder crystalline cornea dystrophy across source vocabularies.
- distrofia corneal cristalina de Schnyder
- distrofia corneal cristalina de Schnyder (trastorno)
- Schnyder crystalline cornea dystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Connective tissue hereditary disorder
- 1Hereditary corneal dystrophy
- 1Stromal corneal dystrophy
- 2Autosomal hereditary disorder
- 2Corneal dystrophy
- 2Corneal stromal degeneration
- 2Disorder of connective tissue
- 2Hereditary disease
- 2Hereditary disorder of the visual system
- 3Corneal degeneration
- 3Corneal stroma finding
- 3Disease
- 3Disorder of soft tissue
- 3Genetic disease
- 3Hereditary disorder by system
- 3Visual system disorder
- 4Clinical finding
- 4Corneal finding
- 4Degenerative disorder of eye
- 4Disorder of body system
- 4Disorder of cornea
- 4Eye / vision finding
- 4General finding of soft tissue
- 5Anomaly of eye
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