OMOP Concept 4246925
Congenital hypoplasia of parietal bone
StandardConditionSNOMED93282000Disorder
Maps from
1
Descendants
0
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 hypoplasia of parietal bone via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 93282000 | Congenital hypoplasia of parietal bone | Non-standard |
Synonyms
Alternative names recorded for Congenital hypoplasia of parietal bone across source vocabularies.
- Congenital hypoplasia of parietal bone (disorder)
- Congenital small parietal bone
- hipoplasia congénita de hueso parietal
- hipoplasia congénita de hueso parietal (trastorno)
- hueso parietal pequeño congénito
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(25)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of parietal bone
- 1Craniofacial microsomia
- 2Congenital abnormality of skull and face bones
- 2Congenital anomaly of skull
- 2Finding of head region
- 3Congenital anomaly of head
- 3Congenital anomaly of skeletal bone
- 3Disorder of skull
- 3Head finding
- 4Clinical finding
- 4Congenital anomaly of musculoskeletal system
- 4Congenital malformation
- 4Disorder of bone
- 4Disorder of bone development
- 4Disorder of head
- 4Skull finding
- 5Bone finding
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Disorder of musculoskeletal system
- 5Disorder of skeletal system
- 6Disorder of body system
- 6Disorder of fetus and/or newborn
- 6Musculoskeletal finding
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