OMOP Concept 4334874
Central areolar choroidal sclerosis
StandardConditionSNOMED231996009Disorder
Maps from
6
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Central areolar choroidal sclerosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 112338 | Central Choroidal Atrophy, Total | Non-standard |
| CIEL | 145963 | Central areolar choroidal sclerosis | Non-standard |
| ICD9CM | 363.54 | Central choroidal atrophy, total | Non-standard |
| Nebraska Lexicon | 231996009 | Central areolar choroidal sclerosis | Non-standard |
| Read | F435200 | Helicoid choroid dystrophy | Non-standard |
| Read | F435400 | Total central choroid atrophy | Non-standard |
Synonyms
Alternative names recorded for Central areolar choroidal sclerosis across source vocabularies.
- Central areolar choroidal dystrophy
- Central areolar choroidal sclerosis (disorder)
- esclerosis coroidea areolar central
- esclerosis coroidea areolar central (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Hereditary choroidal dystrophy
- 1Lesion of eye
- 2Anomaly of eye
- 2Choroidal degeneration
- 2Choroidal dystrophy
- 2Hereditary disorder of the visual system
- 3Degenerative disorder of eye
- 3Disorder of choroid of eye
- 3Disorder of eye
- 3Hereditary disorder by system
- 3Visual system disorder
- 4Choroid finding
- 4Degenerative disorder
- 4Disorder of body system
- 4Disorder of eye region
- 4Disorder of posterior segment of eye
- 4Disorder of sensory organ
- 4Disorder of uveal tract
- 4Eye / vision finding
- 4Globe finding
- 4Hereditary disease
- 5Clinical finding
- 5Disease
- 5Disorder of head
- 5Finding of head region
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