OMOP Concept 4094597
Hemoglobin E disease
StandardConditionSNOMED25065001Disorder
Maps from
3
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Hemoglobin E disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138943 | Haemoglobin E disease | Non-standard |
| Nebraska Lexicon | 25065001 | Haemoglobin E-E disease | Non-standard |
| Read | D107500 | Haemoglobin-E disease | Non-standard |
Synonyms
Alternative names recorded for Hemoglobin E disease across source vocabularies.
- enfermedad por hemoglobina E
- enfermedad por hemoglobina E - E
- enfermedad por hemoglobina E (trastorno)
- Haemoglobin E disease
- Haemoglobin E-E disease
- Hemoglobin E disease (disorder)
- Hemoglobin E-E disease
- Homozygous for Hb E
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Hereditary hemoglobinopathy due to globin chain mutation
- 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
Narrower concepts
(3)Included automatically when you query with descendants.
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