OMOP Concept 4313156
Juvenile retinoschisis
StandardConditionSNOMED86923008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Juvenile retinoschisis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136344 | Juvenile retinoschisis | Non-standard |
| Read | F427300 | Juvenile retinoschisis | Non-standard |
Synonyms
Alternative names recorded for Juvenile retinoschisis across source vocabularies.
- Juvenile retinoschisis (disorder)
- retinosquisis juvenil
- retinosquisis juvenil ligada al cromosoma X
- retinosquisis juvenil (trastorno)
- X-linked foveal retinoschisis
- X-linked retinoschisis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Hereditary retinal dystrophy
- 1Retinoschisis
- 1X-linked recessive hereditary disease
- 2Degeneration of retina
- 2Hereditary disorder of the visual system
- 2Retinal detachment
- 2Retinal dystrophy
- 2X-linked hereditary disease
- 3Degenerative disorder of eye
- 3Hereditary disorder by system
- 3Lesion of retina
- 3Retinal disorder
- 3Sex-linked hereditary disorder
- 3Visual system disorder
- 4Anomaly of eye
- 4Degenerative disorder
- 4Disorder of body system
- 4Disorder of vitreous body and/or retina
- 4Eye / vision finding
- 4Hereditary disease
- 4Lesion of eye
- 4Retina finding
- 5Clinical finding
- 5Disease
- 5Disorder of eye
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