OMOP Concept 4122931
Alpha-beta thalassemia
StandardConditionSNOMED234389001Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Alpha-beta thalassemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234389001 | Alpha-beta thalassemia | Non-standard |
Synonyms
Alternative names recorded for Alpha-beta thalassemia across source vocabularies.
- Alpha-beta thalassaemia
- Alpha-beta thalassemia (disorder)
- talasemia alfa-beta
- talasemia alfa-beta (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Thalassemia
- 2Anemia due to disturbance of hemoglobin synthesis
- 2Hereditary hemoglobinopathy
- 3Anemia
- 3Congenital disease
- 3Hemoglobin below reference range
- 3Hemoglobinopathy
- 3Hereditary red blood cell disorder
- 4Disorder of cellular component of blood
- 4Disorder of fetus and/or newborn
- 4Hemoglobin level outside reference range
- 4Hereditary disorder of cellular element of blood
- 4Measurement finding below reference range
- 4Red blood cell disorder
- 5Disease
- 5Disorder of body system
- 5Finding of blood, lymphatics and immune system
- 5Hematology test outside reference range
- 5Hemoglobin finding
- 5Hereditary disorder by system
- 5Measurement finding outside reference range
- 6Clinical finding
- 6Hematopoietic system finding
- 6Hereditary disease
- 6Measurement finding
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