OMOP Concept 4121113
Alpha thalassemia-2 trait
StandardConditionSNOMED234385007Disorder
Maps from
1
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
1 source code normalizes to Alpha thalassemia-2 trait via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149051 | Alpha thalassaemia 2 | Non-standard |
Synonyms
Alternative names recorded for Alpha thalassemia-2 trait across source vocabularies.
- Alpha thalassaemia-2 trait
- Alpha thalassemia-2 trait (disorder)
- rasgo de alfatalasemia 2
- rasgo de alfatalasemia 2 (trastorno)
- rasgo de talasemia alfa - 2
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.
- 1Alpha thalassemia
- 2Thalassemia
- 3Anemia due to disturbance of hemoglobin synthesis
- 3Hereditary hemoglobinopathy
- 4Anemia
- 4Congenital disease
- 4Hemoglobin below reference range
- 4Hemoglobinopathy
- 4Hereditary red blood cell disorder
- 5Disorder of cellular component of blood
- 5Fetal and/or neonatal disorder
- 5Hemoglobin level outside reference range
- 5Hereditary disorder of cellular element of blood
- 5Measurement finding below reference range
- 5Red blood cell disorder
- 6Disease
- 6Disorder of body system
- 6Finding of blood, lymphatics and immune system
- 6Hematology test outside reference range
- 6Hemoglobin finding
- 6Hereditary disorder by system
- 6Measurement finding outside reference range
- 7Clinical finding
- 7Hematopoietic system finding
- 7Hereditary disease
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