OMOP Concept 4098749
Alpha trait thalassemia
StandardConditionSNOMED191187006Disorder
Maps from
3
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
3 source codes normalize to Alpha trait thalassemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 110532 | Alpha thalassaemia trait | Non-standard |
| Nebraska Lexicon | 191187006 | Alpha trait thalassaemia | Non-standard |
| Read | D104400 | Alpha trait thalassaemia | Non-standard |
Synonyms
Alternative names recorded for Alpha trait thalassemia across source vocabularies.
- alfatalasemia
- Alpha thalassaemia trait
- Alpha thalassemia trait
- Alpha trait thalassaemia
- Alpha trait thalassemia (disorder)
- talasemia de rasgo alfa
- talasemia de rasgo alfa (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Alpha thalassemia
- 1Heterozygous 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
- 5Disorder of fetus and/or newborn
- 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
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