OMOP Concept 45765417
Spondyloepimetaphyseal dysplasia, Strudwick type
StandardConditionSNOMED702350003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Spondyloepimetaphyseal dysplasia, Strudwick type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537501 | Strudwick syndrome | Non-standard |
Synonyms
Alternative names recorded for Spondyloepimetaphyseal dysplasia, Strudwick type across source vocabularies.
- Dappled metaphysis syndrome
- displasia espondiloepimetafisaria, tipo Strudwick
- displasia espondiloepimetafisaria, tipo Strudwick (trastorno)
- SEMD - spondyloepimetaphyseal dysplasia, Strudwick type
- síndrome de metáfisis moteadas
- síndrome de Strudwick
- Spondyloepimetaphyseal dysplasia, Strudwick type (disorder)
- Strudwick syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Osteochondrodysplasia syndrome
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Hereditary disease
- 2Multiple system malformation syndrome
- 3Congenital malformation syndrome
- 3Disease
- 3Genetic disease
- 4Clinical finding
- 4Congenital malformation
- 5Congenital disease
- 6Fetal and/or neonatal disorder
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