OMOP Concept 4259003
Congenital anomaly of organ of Corti
StandardConditionSNOMED44621005Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Congenital anomaly of organ of Corti via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144210 | Congenital anomaly of organ of Corti | Non-standard |
| Nebraska Lexicon | 44621005 | Congenital anomaly of the organ of Corti | Non-standard |
| Read | P405100 | Congenital anomaly of the organ of Corti | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of organ of Corti across source vocabularies.
- anomalía congénita del órgano de Corti
- anomalía congénita del órgano de Corti (trastorno)
- Congenital anomaly of organ of Corti (disorder)
- Congenital anomaly of the organ of Corti
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(44)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of central nervous system
- 1Congenital anomaly of cochlea
- 1Congenital anomaly of skull
- 2Congenital abnormality of skull and face bones
- 2Congenital anomaly of membranous labyrinth
- 2Congenital anomaly of nervous system
- 2Disorder of skull
- 2Disorder of the central nervous system
- 3Central nervous system finding
- 3Congenital anomaly of head
- 3Congenital anomaly of skeletal bone
- 3Congenital anomaly of vestibule of inner ear
- 3Congenital malformation
- 3Disorder of bone
- 3Disorder of head
- 3Disorder of nervous system
- 3Skull finding
- 4Bone finding
- 4Clinical finding
- 4Congenital anomaly of musculoskeletal system
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of bone development
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