OMOP Concept 30978
Thalassemia
StandardConditionSNOMED40108008Disorder
Maps from
38
Descendants
79
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
38 source codes normalize to Thalassemia via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Thalassemia across source vocabularies.
- Hereditary leptocytosis
- talasemia
- talasemia (trastorno)
- Thalassaemia
- Thalassemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Anemia due to disturbance of hemoglobin synthesis
- 1Hereditary hemoglobinopathy
- 2Anemia
- 2Congenital disease
- 2Hemoglobin below reference range
- 2Hemoglobinopathy
- 2Hereditary red blood cell disorder
- 3Disorder of cellular component of blood
- 3Disorder of fetus and/or newborn
- 3Hemoglobin level outside reference range
- 3Hereditary disorder of cellular element of blood
- 3Measurement finding below reference range
- 3Red blood cell disorder
- 4Disease
- 4Disorder of body system
- 4Finding of blood, lymphatics and immune system
- 4Hematology test outside reference range
- 4Hemoglobin finding
- 4Hereditary disorder by system
- 4Measurement finding outside reference range
- 5Clinical finding
- 5Hematopoietic system finding
- 5Hereditary disease
- 5Measurement finding
- 5Protein level - finding
Narrower concepts
(79)Included automatically when you query with descendants.
- 1Acquired hemoglobin H disease
- 1Alpha-beta thalassemia
- 1Alpha thalassemia
- 1Beta thalassemia
- 1Delta thalassemia
- 1Gamma thalassemia
- 1Hb Lepore thalassemia
- 1Hereditary persistence of fetal hemoglobin thalassemia
- 1Heterozygous thalassemia
- 1Thalassemia in mother complicating childbirth
- 1Thalassemia in mother complicating pregnancy
- 1Thalassemia intermedia
- 1Thalassemia major
- 1Thalassemia syndrome
- 1Thalassemia with other hemoglobinopathy
- 2Alpha plus thalassemia
- 2Alpha thalassemia-2 trait
- 2Alpha-thalassemia intellectual disability syndrome linked to chromosome 16
- 2Alpha thalassemia X-linked intellectual disability syndrome
- 2Alpha trait thalassemia
- 2Alpha zero thalassemia
- 2Beta plus thalassemia
- 2Beta thalassemia intermedia
- 2Beta thalassemia trait
- 2Beta thalassemia X-linked thrombocytopenia syndrome
- 2Beta zero thalassemia
- 2Delta-beta-Lepore thalassemia
- 2Delta beta thalassemia
- 2Delta beta thalassemia trait
- 2Delta zero thalassemia
- 2Dominant beta-thalassemia
- 2Hemoglobin Bart's hydrops syndrome
- 2Hemoglobin C beta plus thalassemia
- 2Hemoglobin C/beta thalassemia disease
- 2Hemoglobin C beta zero thalassemia
- 2Hemoglobin Constant Spring trait
- 2Hemoglobin D beta plus thalassemia
- 2Hemoglobin D/beta thalassemia disease
- 2Hemoglobin D beta zero thalassemia
- 2Hemoglobin E beta plus thalassemia
- 2Hemoglobin E/beta thalassemia disease
- 2Hemoglobin E beta zero thalassemia
- 2Hemoglobin H constant spring thalassemia
- 2Hemoglobin H disease
- 2Hemoglobin Lepore trait
- 2Hemoglobin Paksé disease
- 2Hemoglobin Seal Rock disease
- 2Hereditary persistence of fetal hemoglobin delta beta plus thalassemia
- 2Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia
- 2Homozygous alpha thalassemia
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