OMOP Concept 4245337
Congenital anomaly of premaxilla
StandardConditionSNOMED93019008Disorder
Maps from
1
Descendants
10
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 anomaly of premaxilla via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 93019008 | Congenital anomaly of premaxilla | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of premaxilla across source vocabularies.
- anomalía congénita del premaxilar
- anomalía congénita del premaxilar (trastorno)
- Congenital anomaly of premaxilla (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of fetal head bones
- 1Finding of head region
- 2Congenital anomaly of head
- 2Congenital anomaly of skeletal bone
- 2Disorder of embryonic structure
- 2Head finding
- 3Clinical finding
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Disease
- 3Disorder of bone development
- 3Disorder of head
- 4Congenital disease
- 4Developmental disorder
- 4Disorder of bone
- 4Disorder of musculoskeletal system
- 5Bone finding
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
- 5Disorder of skeletal system
- 5Musculoskeletal finding
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Congenital abnormal fusion of premaxilla
- 1Congenital abnormal shape of premaxilla
- 1Congenital absence of premaxilla
- 1Congenital fenestration of premaxilla
- 1Congenital hypoplasia of premaxilla
- 1Incomplete ossification of premaxilla
- 1Lack of ossification of premaxilla
- 2Aplasia of premaxilla
- 2Vomero-premaxillary faciosynostosis
- 3Agenesis of premaxilla
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