OMOP Concept 4048205
Homozygous hemoglobinopathy
StandardConditionSNOMED123772008Disorder
Maps from
1
Descendants
13
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 Homozygous hemoglobinopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 123772008 | Homozygous haemoglobinopathy | Non-standard |
Synonyms
Alternative names recorded for Homozygous hemoglobinopathy across source vocabularies.
- hemoglobinopatía homocigótica
- hemoglobinopatía homocigótica (trastorno)
- Homozygous haemoglobinopathy
- Homozygous hemoglobinopathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Hereditary hemoglobinopathy
- 2Congenital disease
- 2Hemoglobinopathy
- 2Hereditary red blood cell disorder
- 3Disorder of fetus and/or newborn
- 3Hereditary disorder of cellular element of blood
- 3Red blood cell disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of cellular component of blood
- 4Hereditary disorder by system
- 5Clinical finding
- 5Finding of blood, lymphatics and immune system
- 5Hereditary disease
- 6Genetic disease
Narrower concepts
(13)Included automatically when you query with descendants.
- 1Sickle cell-hemoglobin SS disease
- 1Vaso-occlusive pain episode in sickle cell disease
- 2Hemoglobin SS disease with crisis
- 2Hemoglobin SS disease without crisis
- 2Sickle cell anemia in mother complicating childbirth
- 2Sickle cell anemia with coexistent alpha-thalassemia
- 2Sickle cell anemia with high hemoglobin F
- 3Acute sickle cell splenic sequestration crisis
- 3Hemoglobin SS disease with vasoocclusive crisis
- 3Sickle cell crisis with extensive hemolysis
- 3Vasoocclusive sickle cell crisis
- 4Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis
- 4Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis
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