OMOP Concept 37109698
Reticular dystrophy of retinal pigment epithelium
StandardConditionSNOMED723502001Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Reticular dystrophy of retinal pigment epithelium via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566721 | Reticular Dystrophy Of Retinal Pigment Epithelium | Non-standard |
| Nebraska Lexicon | 723502001 | Reticular dystrophy of retinal pigment epithelium | Non-standard |
Synonyms
Alternative names recorded for Reticular dystrophy of retinal pigment epithelium across source vocabularies.
- distrofia reticular de epitelio pigmentario de la retina
- distrofia reticular de epitelio pigmentario de la retina (trastorno)
- Reticular dystrophy of retinal pigment epithelium (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hereditary retinal dystrophy
- 1Retinal pigment epithelial dystrophy
- 2Autosomal hereditary disorder
- 2Hereditary disorder of the visual system
- 2Retinal dystrophy
- 2Retinal pigment epithelial abnormality
- 3Anomaly of eye
- 3Degeneration of retina
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Retinal disorder
- 3Visual system disorder
- 4Degenerative disorder of eye
- 4Disorder of body system
- 4Disorder of eye
- 4Disorder of vitreous body and/or retina
- 4Eye / vision finding
- 4Genetic disease
- 4Retina finding
- 5Clinical finding
- 5Degenerative disorder
- 5Disease
- 5Disorder of eye region
- 5Disorder of posterior segment of eye
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