OMOP Concept 4050933
FH: Congenital RS anomaly
StandardObservationSNOMED160421002Context-dependent
Maps from
2
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to FH: Congenital RS anomaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 160421002 | Family history of congenital respiratory system anomaly | Non-standard |
| Read | 12J4.00 | FH: Congenital RS anomaly | Non-standard |
Synonyms
Alternative names recorded for FH: Congenital RS anomaly across source vocabularies.
- antecedente familiar de anomalía congénita del aparato respiratorio
- antecedente familiar de anomalía congénita del aparato respiratorio (situación)
- Family history: Congenital RS anomaly
- Family history of congenital respiratory system anomaly
- Family history of congenital respiratory system anomaly (situation)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
- 1Family history of congenital malformation
- 1FH: Respiratory disease
- 2Family history of congenital disease
- 2Family history of development disorder
- 2Family history of disorder
- 3Family history of clinical finding
- 4Family history with explicit context
- 4Finding with explicit context
- 5Family History
- 5Situation with explicit context
Narrower concepts
(1)Included automatically when you query with descendants.
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