OMOP Concept 4100891
Congenital heterochromia iridis
StandardConditionSNOMED253234004Disorder
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 Congenital heterochromia iridis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 110366 | Congenital Heterochromia | Non-standard |
| Nebraska Lexicon | 253234004 | Congenital heterochromia iridis | Non-standard |
Synonyms
Alternative names recorded for Congenital heterochromia iridis across source vocabularies.
- Congenital heterochromia iridis (disorder)
- heterocromía congénita del iris
- heterocromía congénita del iris (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of iris
- 2Congenital anomaly of anterior segment of eye
- 2Disorder of iris
- 3Congenital anomaly of eye
- 3Disorder of anterior segment of eye
- 3Disorder of anterior uveal tract
- 3Iris finding
- 4Anomaly of eye
- 4Anterior segment finding
- 4Congenital anomaly of head
- 4Congenital anomaly of visual system
- 4Disorder of eye
- 4Disorder of uveal tract
- 5Congenital malformation
- 5Disorder of eye region
- 5Disorder of head
- 5Disorder of sensory organ
- 5Globe finding
- 5Visual system disorder
- 6Congenital disease
- 6Developmental disorder
- 6Disease
- 6Disorder of body system
- 6Eye / vision finding
- 6Finding of head region
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