OMOP Concept 4305417
Brachyolmia - Maroteaux type
StandardConditionSNOMED389165004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Brachyolmia - Maroteaux type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563218 | Brachyolmia Type 2 | Non-standard |
Synonyms
Alternative names recorded for Brachyolmia - Maroteaux type across source vocabularies.
- Brachyolmia - Maroteaux type (disorder)
- braquiolmia - tipo Maroteaux
- braquiolmia - tipo Maroteaux (trastorno)
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 recessive 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
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