OMOP Concept 44782850
Hereditary retinal dystrophy primarily involving retinal pigment epithelium
StandardConditionSNOMED698847000Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary retinal dystrophy primarily involving retinal pigment epithelium via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 698847000 | Hereditary retinal dystrophy primarily involving retinal pigment epithelium | Non-standard |
Synonyms
Alternative names recorded for Hereditary retinal dystrophy primarily involving retinal pigment epithelium across source vocabularies.
- distrofia hereditaria de la retina que afecta principalmente al epitelio pigmentario
- distrofia hereditaria de la retina que afecta principalmente al epitelio pigmentario (trastorno)
- Hereditary retinal dystrophy primarily involving retinal pigment epithelium (disorder)
- Inherited retinal dystrophy primarily involving retinal pigment epithelium
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Hereditary retinal dystrophy
- 2Hereditary disorder of the visual system
- 2Retinal dystrophy
- 3Degeneration of retina
- 3Hereditary disorder by system
- 3Visual system disorder
- 4Degenerative disorder of eye
- 4Disorder of body system
- 4Eye / vision finding
- 4Hereditary disease
- 4Retinal disorder
- 5Anomaly of eye
- 5Clinical finding
- 5Degenerative disorder
- 5Disease
- 5Disorder of vitreous body and/or retina
- 5Genetic disease
- 5Retina finding
- 6Disorder of eye
- 6Disorder of posterior segment of eye
- 6Globe finding
- 7Disorder of eye region
- 7Disorder of sensory organ
- 7Finding of head region
- 8Disorder of head
Narrower concepts
(1)Included automatically when you query with descendants.
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