OMOP Concept 4050934
Family history of chromosomal anomaly
StandardObservationSNOMED160425006Context-dependent
Maps from
2
Descendants
11
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 Family history of chromosomal anomaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 160425006 | Family history: Chromosomal anomaly | Non-standard |
| Read | 12J8.00 | FH: Chromosomal anomaly | Non-standard |
Synonyms
Alternative names recorded for Family history of chromosomal anomaly across source vocabularies.
- antecedente familiar de anomalía cromosómica
- antecedente familiar de anomalía cromosómica (situación)
- Family history of chromosomal anomaly (situation)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(11)Included automatically when you query with descendants.
- 1Family history of complete trisomy 21 syndrome
- 1Family history of Downs syndrome
- 1Family history of fragile X syndrome
- 1Family history of fragile X syndrome in first degree relative
- 1Family history of sex chromosome aneuploidy
- 1Family history of sex chromosome translocation
- 1Family history of trisomy 13
- 1Family history of trisomy 18
- 1Family history of Turner syndrome
- 1Family history of velocardiofacial syndrome
- 2Family history of trisomy 18 syndrome
Get this concept via the API
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