OMOP Concept 760844
Homozygous hemoglobin H constant spring thalassemia
StandardConditionSNOMED119641000119103Disorder
Maps from
1
Descendants
0
Valid from
1 Mar 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Homozygous hemoglobin H constant spring thalassemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 119641000119103 | Homozygous hemoglobin H constant spring thalassemia | Non-standard |
Synonyms
Alternative names recorded for Homozygous hemoglobin H constant spring thalassemia across source vocabularies.
- Homozygous hemoglobin H constant spring thalassemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Hemoglobin H constant spring thalassemia
- 2Alpha thalassemia
- 3Thalassemia
- 4Anemia due to disturbance of hemoglobin synthesis
- 4Hereditary hemoglobinopathy
- 5Anemia
- 5Congenital disease
- 5Hemoglobin below reference range
- 5Hemoglobinopathy
- 5Hereditary red blood cell disorder
- 6Disorder of cellular component of blood
- 6Disorder of fetus and/or newborn
- 6Hemoglobin level outside reference range
- 6Hereditary disorder of cellular element of blood
- 6Measurement finding below reference range
- 6Red blood cell disorder
- 7Disease
- 7Disorder of body system
- 7Finding of blood, lymphatics and immune system
- 7Hematology test outside reference range
- 7Hemoglobin finding
- 7Hereditary disorder by system
- 7Measurement finding outside reference range
- 8Clinical finding
- 8Hematopoietic system finding
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