OMOP Concept 4047524
Heterozygous hemoglobinopathy
StandardConditionSNOMED123773003Disorder
Maps from
1
Descendants
8
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Heterozygous hemoglobinopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 123773003 | Heterozygous haemoglobinopathy | Non-standard |
Synonyms
Alternative names recorded for Heterozygous hemoglobinopathy across source vocabularies.
- hemoglobinopatía heterocigota
- hemoglobinopatía heterocigótica
- hemoglobinopatía heterocigótica (trastorno)
- Heterozygous haemoglobinopathy
- Heterozygous hemoglobinopathy (disorder)
- Trait haemoglobinopathy
- Trait hemoglobinopathy
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
(8)Included automatically when you query with descendants.
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