OMOP Concept 4130678
Sickle cell beta plus thalassemia
StandardConditionSNOMED127042006Disorder
Maps from
8
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
8 source codes normalize to Sickle cell beta plus thalassemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | D57.44 | Sickle-cell thalassemia beta plus without crisis | Non-standard |
| ICD10CM | D57.45 | Sickle-cell thalassemia beta plus with crisis | Non-standard |
| ICD10CM | D57.451 | Sickle-cell thalassemia beta plus with acute chest syndrome | Non-standard |
| ICD10CM | D57.452 | Sickle-cell thalassemia beta plus with splenic sequestration | Non-standard |
| ICD10CM | D57.453 | Sickle-cell thalassemia beta plus with cerebral vascular involvement | Non-standard |
| ICD10CM | D57.454 | Sickle-cell thalassemia beta plus with dactylitis | Non-standard |
| ICD10CM | D57.458 | Sickle-cell thalassemia beta plus with crisis with other specified complication | Non-standard |
| ICD10CM | D57.459 | Sickle-cell thalassemia beta plus with crisis, unspecified | Non-standard |
Synonyms
Alternative names recorded for Sickle cell beta plus thalassemia across source vocabularies.
- Sickle cell beta plus thalassaemia
- Sickle cell beta plus thalassemia (disorder)
- talasemia beta más de células drepanocíticas
- talasemia beta más de células drepanocíticas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Beta plus thalassemia
- 1Sickle cell-beta-thalassemia
- 2Beta 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
- 6Fetal and/or neonatal disorder
- 6Hemoglobin level outside reference range
- 6Hereditary disorder of cellular element of blood
Showing 25 of 40. Retrieve the full set via the API.
Get this concept via the API
Resolve Sickle cell beta plus thalassemia - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4130678?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card