OMOP Concept 436410
Lattice corneal dystrophy, isolated form
StandardConditionSNOMED231933003Disorder
Maps from
1
Descendants
0
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 Lattice corneal dystrophy, isolated form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 231933003 | Lattice corneal dystrophy, isolated form | Non-standard |
Synonyms
Alternative names recorded for Lattice corneal dystrophy, isolated form across source vocabularies.
- distrofia corneana de Lattice, forma aislada
- distrofia corneana de Lattice, forma aislada (trastorno)
- Lattice corneal dystrophy, isolated form (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1Congenital macular corneal dystrophy
- 2Congenital connective tissue disorder
- 2Congenital corneal dystrophy
- 2Macular corneal dystrophy
- 3Autosomal recessive hereditary disorder
- 3Congenital disease
- 3Congenital structural abnormality of cornea
- 3Connective tissue hereditary disorder
- 3Corneal dystrophy
- 3Developmental hereditary disorder
- 3Disorder of connective tissue
- 3Hereditary corneal dystrophy
- 3Stromal corneal dystrophy
- 4Autosomal hereditary disorder
- 4Congenital anomaly of anterior segment of eye
- 4Corneal degeneration
- 4Corneal stromal degeneration
- 4Developmental disorder
- 4Disease
- 4Disorder of cornea
- 4Disorder of fetus and/or newborn
- 4Hereditary disease
- 4Hereditary disorder of the visual system
- 5Clinical finding
- 5Congenital anomaly of eye
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