OMOP Concept 45773359
Spondyloperipheral dysplasia
StandardConditionSNOMED702339001Disorder
Maps from
1
Descendants
1
Valid from
31 Jul 2014
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Spondyloperipheral dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535799 | Spondyloperipheral dysplasia short ulna | Non-standard |
Synonyms
Alternative names recorded for Spondyloperipheral dysplasia across source vocabularies.
- displasia espondiloperiférica
- displasia espondiloperiférica (trastorno)
- Spondyloperipheral dysplasia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of skeletal bone
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Lesion of bone
- 1Osteochondrodysplasia syndrome
- 1Skeletal dysplasia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of musculoskeletal system
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 2Structural abnormality of skeleton
- 3Bone finding
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Disorder of skeletal system
- 3Genetic disease
- 3Musculoskeletal finding
Showing 25 of 28. Retrieve the full set via the API.
Narrower concepts
(1)Included automatically when you query with descendants.
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