OMOP Concept 46273448
Family history of osteogenesis imperfecta
StandardObservationSNOMED98041000119107Context-dependent
Maps from
1
Descendants
0
Valid from
31 Jul 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Family history of osteogenesis imperfecta via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 98041000119107 | Family history of osteogenesis imperfecta | Non-standard |
Synonyms
Alternative names recorded for Family history of osteogenesis imperfecta across source vocabularies.
- antecedente familiar de osteogénesis imperfecta
- antecedente familiar de osteogénesis imperfecta (situación)
- Family history of osteogenesis imperfecta (situation)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1FH: Cong. orthopedic anomaly
- 2Family history of congenital malformation
- 2FH: Musculoskeletal disease
- 3Family history of congenital disease
- 3Family history of development disorder
- 3Family history of disorder
- 3Have you or anyone in your family ever been diagnosed with the following bone, joint, and muscle conditions? Think only of the people you are related to by blood. Select all that apply.
- 4Family history of clinical finding
- 4Family Members Diagnosed: Diagnosed Health Condition
- 5Family history with explicit context
- 5Finding with explicit context
- 6Family History
- 6Situation with explicit context
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