OMOP Concept 4109972
Spondyloenchondrodysplasia
StandardConditionSNOMED254079002Disorder
Maps from
1
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Spondyloenchondrodysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535782 | Spondyloenchondrodysplasia | Non-standard |
Synonyms
Alternative names recorded for Spondyloenchondrodysplasia across source vocabularies.
- espondiloencondrodisplasia
- espondiloencondrodisplasia (trastorno)
- Spondyloenchondrodysplasia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(46)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of immune system
- 1Hereditary disorder of musculoskeletal system
- 1Metaphyseal chondrodysplasia
- 1Type I interferonopathy
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Congenital malformation syndromes associated with short stature
- 2Developmental disorder
- 2Disorder of immune function
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of bone
- 2Monogenic autoinflammatory syndrome
- 2Skeletal dysplasia
- 3Autoinflammatory disease
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Disorder of bone
- 3Disorder of bone development
- 3Genetic disease
Showing 25 of 46. Retrieve the full set via the API.
Narrower concepts
(1)Included automatically when you query with descendants.
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