OMOP Concept 4336142
Congenital color blindness
StandardConditionSNOMED232148006Disorder
Maps from
1
Descendants
7
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 Congenital color blindness via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 232148006 | Congenital colour blindness | Non-standard |
Synonyms
Alternative names recorded for Congenital color blindness across source vocabularies.
- ceguera a los colores congénita
- ceguera a los colores congénita (trastorno)
- Congenital color blindness (disorder)
- Congenital colour blindness
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Color blindness
- 1Color vision deficiency
- 1Congenital disease
- 2Disorder of fetus and/or newborn
- 2Disorder of vision
- 2Retinal disorder
- 2Visual disturbance
- 3Disease
- 3Disorder of vitreous body and/or retina
- 3Retina finding
- 3Visual system disorder
- 4Clinical finding
- 4Disorder of body system
- 4Disorder of posterior segment of eye
- 4Eye / vision finding
- 4Globe finding
- 5Disorder of eye
- 5Finding of head region
- 6Disorder of eye region
- 6Disorder of sensory organ
- 6Head finding
- 7Disorder of head
Narrower concepts
(7)Included automatically when you query with descendants.
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