OMOP Concept 4334253
Hereditary vitreoretinopathy
StandardConditionSNOMED232062002Disorder
Maps from
1
Descendants
6
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 Hereditary vitreoretinopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 232062002 | Hereditary vitreoretinopathy | Non-standard |
Synonyms
Alternative names recorded for Hereditary vitreoretinopathy across source vocabularies.
- Hereditary vitreoretinopathy (disorder)
- vitreorretinopatía hereditaria
- vitreorretinopatía hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(31)Roll up to these when you need a wider cohort.
- 1Connective tissue hereditary disorder
- 1Disorder of vitreous body
- 1Hereditary disorder of the visual system
- 1Retinal disorder
- 2Disorder of connective tissue
- 2Disorder of ocular adnexa
- 2Disorder of orbit proper
- 2Disorder of soft tissue of head
- 2Disorder of vitreous body and/or retina
- 2Disorder of vitreous cavity
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Retina finding
- 2Visual system disorder
- 3Disease
- 3Disorder of body system
- 3Disorder of eye region
- 3Disorder of head
- 3Disorder of posterior segment of eye
- 3Disorder of soft tissue
- 3Eye / vision finding
- 3Genetic disease
- 3Globe finding
- 3Orbit finding
- 3Vitreous cavity finding
Narrower concepts
(6)Included automatically when you query with descendants.
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