OMOP Concept 4032709
Congenital alveolar hypoplasia of maxilla
StandardConditionSNOMED109527002Disorder
Maps from
1
Descendants
0
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 alveolar hypoplasia of maxilla via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 109527002 | Congenital alveolar hypoplasia of maxilla | Non-standard |
Synonyms
Alternative names recorded for Congenital alveolar hypoplasia of maxilla across source vocabularies.
- Congenital alveolar hypoplasia of maxilla (disorder)
- Congenital maxillary alveolar hypoplasia
- hipoplasia alveolar congénita del maxilar
- hipoplasia alveolar congénita del maxilar superior
- hipoplasia alveolar congénita del maxilar (trastorno)
- hipoplasia alveolar maxilar congénita
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(58)Roll up to these when you need a wider cohort.
- 1Congenital abnormality of oral cavity
- 1Congenital anomaly of digestive organ
- 1Congenital maxillary hypoplasia
- 1Maxillary alveolar hypoplasia
- 2Alveolar ridge abnormality of maxilla
- 2Congenital anomaly of digestive system
- 2Congenital anomaly of maxilla
- 2Congenital anomaly of mouth
- 2Craniofacial microsomia
- 2Disorder of digestive organ
- 2Hypoplasia of maxillary bone
- 2Oral cavity finding
- 3Alveolar ridge abnormality
- 3Congenital abnormality of skull and face bones
- 3Congenital anomaly of face bones
- 3Congenital anomaly of head
- 3Congenital anomaly of jaw
- 3Congenital anomaly of skull
- 3Congenital malformation
- 3Congenital malformation of upper alimentary tract
- 3Disease of mouth
- 3Disorder of digestive system
- 3Disorder of digestive system specific to fetus OR newborn
- 3Disorder of maxilla
- 3Finding of mouth region
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