OMOP Concept 4130189
Sickle cell trait with coexistent alpha-thalassemia
StandardConditionSNOMED127046009Disorder
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 Sickle cell trait with coexistent alpha-thalassemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 127046009 | Sickle cell trait with coexistent alpha-thalassaemia | Non-standard |
Synonyms
Alternative names recorded for Sickle cell trait with coexistent alpha-thalassemia across source vocabularies.
- rasgo de células drepanocíticas con talasemia - alfa concomitante
- rasgo de células drepanocíticas con talasemia - alfa concomitante (trastorno)
- Sickle cell trait with coexistent alpha-thalassaemia
- Sickle cell trait with coexistent alpha-thalassemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Alpha thalassemia
- 1Sickle cell trait
- 2Hereditary hemoglobin S
- 2Heterozygous hemoglobinopathy
- 2Thalassemia
- 3Anemia due to disturbance of hemoglobin synthesis
- 3Hereditary hemoglobinopathy
- 3Hereditary hemoglobinopathy due to globin chain mutation
- 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
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