OMOP Concept 37397206
Autosomal dominant brachyolmia
StandardConditionSNOMED717264003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant brachyolmia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562963 | Brachyolmia Type 3 | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant brachyolmia across source vocabularies.
- Autosomal dominant brachyolmia (disorder)
- Brachyolmia type 3
- braquiolmia autosómica dominante
- braquiolmia autosómica dominante (trastorno)
- braquiolmia tipo 3
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(37)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Brachyolmia
- 2Autosomal hereditary disorder
- 2Congenital malformation syndromes associated with short stature
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Spondylodysplastic group
- 3Congenital anomaly of skeletal bone
- 3Congenital malformation syndrome
- 3Developmental disorder
- 3Disorder of musculoskeletal system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Lesion of bone
- 3Short stature disorder
- 3Skeletal dysplasia
- 4Congenital anomaly of musculoskeletal system
- 4Congenital malformation
- 4Disease
- 4Disorder of body system
- 4Disorder of bone
- 4Disorder of bone development
- 4Disorder of stature
- 4Genetic disease
- 4Musculoskeletal finding
Showing 25 of 37. Retrieve the full set via the API.
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