OMOP Concept 4131914
Sickle cell anemia with coexistent alpha-thalassemia
StandardConditionSNOMED127045008Disorder
Maps from
0
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Sickle cell anemia with coexistent alpha-thalassemia across source vocabularies.
- anemia drepanocítica con talasemia - alfa concomitante
- anemia drepanocítica con talasemia - alfa concomitante (trastorno)
- Sickle cell anaemia with coexistent alpha-thalassaemia
- Sickle cell anemia with coexistent alpha-thalassemia (disorder)
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.
- 1Alpha thalassemia
- 1Sickle cell-hemoglobin SS disease
- 1Sickle cell-thalassemia disease
- 2Anemia due to disturbance of hemoglobin synthesis
- 2Anemia due to intrinsic red cell abnormality
- 2Disorder of hematopoietic structure
- 2Homozygous hemoglobinopathy
- 2Sickling disorder due to hemoglobin S
- 2Thalassemia
- 2Thalassemia with other hemoglobinopathy
- 3Anemia
- 3Disorder of body system
- 3Hemoglobin below reference range
- 3Hereditary hemoglobinopathy
- 3Hereditary hemoglobin S
- 4Congenital disease
- 4Disease
- 4Disorder of cellular component of blood
- 4Hemoglobin level outside reference range
- 4Hemoglobinopathy
- 4Hereditary hemoglobinopathy due to globin chain mutation
- 4Hereditary red blood cell disorder
- 4Measurement finding below reference range
- 5Clinical finding
- 5Fetal and/or neonatal disorder
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