OMOP Concept 45757282
Congenital anomaly of pupil
StandardConditionSNOMED11211000119108Disorder
Maps from
1
Descendants
15
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital anomaly of pupil via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 11211000119108 | Congenital anomaly of pupil | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of pupil across source vocabularies.
- anomalía congénita de pupila
- anomalía congénita de pupila (trastorno)
- Congenital anomaly of pupil (disorder)
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.
- 1Congenital anomaly of eye
- 1Pupillary disorder
- 2Anomaly of eye
- 2Congenital anomaly of head
- 2Congenital anomaly of visual system
- 2Disorder of eye
- 2Pupil finding
- 3Congenital malformation
- 3Disorder of eye region
- 3Disorder of head
- 3Disorder of sensory organ
- 3Globe finding
- 3Visual system disorder
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of body system
- 4Eye / vision finding
- 4Finding of head region
- 4Head finding
- 5Clinical finding
- 5Disorder of fetus and/or newborn
Narrower concepts
(15)Included automatically when you query with descendants.
- 1Atresia of pupil
- 1Congenital anisocoria
- 1Congenital anomaly of left pupil
- 1Congenital anomaly of right pupil
- 1Congenital ectopic pupil
- 1Congenital miosis
- 1Congenital mydriasis
- 1Persistent pupillary membranes
- 2Bilateral congenital anomaly of pupil
- 2Persistent pupillary membranes, iris to cornea
- 2Persistent pupillary membranes, iris to iris
- 2Persistent pupillary membranes, iris to lens
- 2Ptosis, strabismus, ectopic pupil syndrome
- 2Spastic ataxia with congenital miosis
- 2Thrombocytopathy, asplenia and miosis
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