OMOP Concept 4245329
Congenital anomaly of basisphenoid bone
StandardConditionSNOMED92996006Disorder
Maps from
1
Descendants
7
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Congenital anomaly of basisphenoid bone via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 92996006 | Congenital anomaly of basisphenoid bone | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of basisphenoid bone across source vocabularies.
- anomalía congénita de hueso basiesfenoidal
- anomalía congénita de hueso basiesfenoidal (trastorno)
- Congenital anomaly of basisphenoid bone (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of fetal head bones
- 2Congenital anomaly of head
- 2Congenital anomaly of skeletal bone
- 2Disorder of embryonic structure
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Disease
- 3Disorder of bone development
- 3Disorder of head
- 4Clinical finding
- 4Congenital disease
- 4Developmental disorder
- 4Disorder of bone
- 4Disorder of musculoskeletal system
- 4Head finding
- 5Bone finding
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
- 5Disorder of skeletal system
- 5Musculoskeletal finding
Narrower concepts
(7)Included automatically when you query with descendants.
- 1Congenital abnormal fusion of basisphenoid bone
- 1Congenital abnormal shape of basisphenoid bone
- 1Congenital absence of basisphenoid bone
- 1Congenital fenestration of basisphenoid bone
- 1Congenital hypoplasia of basisphenoid bone
- 1Incomplete ossification of basisphenoid bone
- 1Lack of ossification of basisphenoid bone
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