OMOP Concept 4091092
Osteogenesis imperfecta, type IV B
StandardConditionSNOMED279309008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Osteogenesis imperfecta, type IV B via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 131632 | Osteogenesis imperfecta, type IV B | Non-standard |
| Nebraska Lexicon | 279309008 | Osteogenesis imperfecta, type IV B | Non-standard |
Synonyms
Alternative names recorded for Osteogenesis imperfecta, type IV B across source vocabularies.
- osteogénesis imperfecta tipo IV B
- osteogénesis imperfecta tipo IV B (trastorno)
- osteogénesis imperfecta tipo IV con dentinogénesis imperfecta
- Osteogenesis imperfecta, type IV B (disorder)
- Osteogenesis imperfecta type IV with dentinogenesis imperfecta
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(58)Roll up to these when you need a wider cohort.
- 1Dentinogenesis imperfecta
- 1Hereditary disorder of musculoskeletal system
- 1Osteogenesis imperfecta with normal sclerae, dominant form
- 2Autosomal dominant hereditary disorder
- 2Congenital anomaly of tooth
- 2Developmental hereditary disorder
- 2Disorder of hard tissues of teeth
- 2Disorder of musculoskeletal system
- 2Hereditary disorder by system
- 2Hereditary disorder of tooth
- 2Osteogenesis imperfecta
- 3Abnormal bone formation
- 3Autosomal hereditary disorder
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Congenital anomaly of skeletal bone
- 3Developmental disorder
- 3Digestive system hereditary disorder
- 3Disorder of body system
- 3Genetic disease
- 3Hereditary disease
- 3Malformation of tooth
- 3Musculoskeletal finding
- 3Skeletal dysplasia
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