OMOP Concept 4131913
Sickle cell-delta beta0-thalassemia
StandardConditionSNOMED127044007Disorder
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-delta beta0-thalassemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 127044007 | Sickle cell-delta beta^0^-thalassaemia | Non-standard |
Synonyms
Alternative names recorded for Sickle cell-delta beta0-thalassemia across source vocabularies.
- Sickle cell-delta beta^0^-thalassaemia
- Sickle cell-delta beta^0^-thalassemia
- Sickle cell-delta beta^0^-thalassemia (disorder)
- Sickle cell-delta beta<sup>0</sup>-thalassemia
- talasemia - delta beta^0^ de células drepanocíticas
- talasemia - delta beta0 de células drepanocíticas
- talasemia - delta beta^0^ de células drepanocíticas (trastorno)
- talasemia - delta beta<sup>0</sup> de células drepanocíticas
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Delta beta zero thalassemia
- 1Sickle cell-beta-thalassemia
- 2Beta thalassemia
- 2Beta zero thalassemia
- 2Delta beta thalassemia
- 2Double heterozygous sickling disorder
- 2Sickle cell-thalassemia disease
- 3Disorder of hematopoietic structure
- 3Sickling disorder due to hemoglobin S
- 3Thalassemia
- 3Thalassemia with other hemoglobinopathy
- 4Anemia due to disturbance of hemoglobin synthesis
- 4Disorder of body system
- 4Hereditary hemoglobinopathy
- 4Hereditary hemoglobin S
- 5Anemia
- 5Congenital disease
- 5Disease
- 5Hemoglobin below reference range
- 5Hemoglobinopathy
- 5Hereditary hemoglobinopathy due to globin chain mutation
- 5Hereditary red blood cell disorder
- 6Clinical finding
- 6Disorder of cellular component of blood
- 6Disorder of fetus and/or newborn
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