OMOP Concept 4109176
Brachyolmia
StandardConditionSNOMED254088006Disorder
Maps from
1
Descendants
4
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 Brachyolmia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537098 | Brachyolmia | Non-standard |
Synonyms
Alternative names recorded for Brachyolmia across source vocabularies.
- Brachyolmia (disorder)
- braquiolmia
- braquiolmia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Congenital malformation syndromes associated with short stature
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Spondylodysplastic group
- 2Congenital anomaly of skeletal bone
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of bone
- 2Short stature disorder
- 2Skeletal dysplasia
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3Disorder of bone
- 3Disorder of bone development
- 3Disorder of stature
- 3Genetic disease
- 3Musculoskeletal finding
- 3Short stature
- 3Structural abnormality of skeleton
Showing 25 of 35. Retrieve the full set via the API.
Narrower concepts
(4)Included automatically when you query with descendants.
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