OMOP Concept 604590
Osteogenesis imperfecta type 5
StandardConditionSNOMED1003379004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Osteogenesis imperfecta type 5 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567042 | Osteogenesis Imperfecta, Type V | Non-standard |
Synonyms
Alternative names recorded for Osteogenesis imperfecta type 5 across source vocabularies.
- osteogénesis imperfecta tipo 5
- osteogénesis imperfecta tipo 5 (trastorno)
- osteogénesis imperfecta tipo V
- Osteogenesis imperfecta type 5 (disorder)
- Osteogenesis imperfecta type V
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(31)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Osteogenesis imperfecta
- 1Short stature disorder
- 2Abnormal bone formation
- 2Congenital anomaly of skeletal bone
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Disorder of stature
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Skeletal dysplasia
- 3Bone finding
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of bone development
- 3Disorder of skeletal system
- 3Finding of general physiological development
- 3Functional finding
- 3General finding of height
- 3Musculoskeletal finding
- 4Clinical finding
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