OMOP Concept 36714082
Spondyloepimetaphyseal dysplasia Missouri type
StandardConditionSNOMED719171005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Spondyloepimetaphyseal dysplasia Missouri type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566574 | Spondyloepimetaphyseal Dysplasia, Missouri Type | Non-standard |
Synonyms
Alternative names recorded for Spondyloepimetaphyseal dysplasia Missouri type across source vocabularies.
- displasia espondilometafisaria tipo Missouri
- displasia espondilometafisaria tipo Missouri (trastorno)
- Spondyloepimetaphyseal dysplasia Missouri type (disorder)
- Spondyloepimetaphyseal dysplasia type 2
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
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Spondyloepimetaphyseal disorder
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Metaphyseal chondrodysplasia
- 3Congenital anomaly of skeletal bone
- 3Congenital malformation syndromes associated with short stature
- 3Disease
- 3Disorder of body system
- 3Genetic disease
- 3Lesion of bone
- 3Musculoskeletal finding
- 3Skeletal dysplasia
- 4Clinical finding
- 4Congenital anomaly of musculoskeletal system
- 4Congenital malformation syndrome
- 4Disorder of bone
- 4Disorder of bone development
- 4Short stature disorder
- 4Structural abnormality of skeleton
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