OMOP Concept 40484201
Hemoglobin O-Arab trait
StandardConditionSNOMED445542007Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2010
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hemoglobin O-Arab trait via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 445542007 | Haemoglobin O-Arab trait | Non-standard |
Synonyms
Alternative names recorded for Hemoglobin O-Arab trait across source vocabularies.
- Haemoglobin O-Arab trait
- Hemoglobin O-Arab trait (disorder)
- rasgo de hemoglobina O Arab
- rasgo de hemoglobina O Arab (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Hereditary hemoglobinopathy due to globin chain mutation
- 1Heterozygous hemoglobinopathy
- 2Hereditary hemoglobinopathy
- 3Congenital disease
- 3Hemoglobinopathy
- 3Hereditary red blood cell disorder
- 4Disorder of fetus and/or newborn
- 4Hereditary disorder of cellular element of blood
- 4Red blood cell disorder
- 5Disease
- 5Disorder of body system
- 5Disorder of cellular component of blood
- 5Hereditary disorder by system
- 6Clinical finding
- 6Finding of blood, lymphatics and immune system
- 6Hereditary disease
- 7Genetic disease
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