OMOP Concept 4211932
Sickle cell-hemoglobin E disease without crisis
StandardConditionSNOMED416638004Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2005
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Sickle cell-hemoglobin E disease without crisis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 416638004 | Sickle cell-haemoglobin E disease without crisis | Non-standard |
Synonyms
Alternative names recorded for Sickle cell-hemoglobin E disease without crisis across source vocabularies.
- drepanocitosis-enfermedad de la hemoglobina E sin crisis hemolítica
- drepanocitosis-enfermedad de la hemoglobina E sin crisis hemolítica (trastorno)
- Sickle cell-haemoglobin E disease without crisis
- Sickle cell-hemoglobin E disease without crisis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Hemoglobin S sickling disorder without crisis
- 1Sickle cell-hemoglobin E disease
- 2Double heterozygous sickling disorder
- 2Mixed hemoglobin disorder
- 2Sickling disorder due to hemoglobin S
- 3Hemoglobinopathy
- 3Hereditary hemoglobin S
- 4Hereditary hemoglobinopathy due to globin chain mutation
- 4Red blood cell disorder
- 5Disorder of body system
- 5Disorder of cellular component of blood
- 5Hereditary hemoglobinopathy
- 6Congenital disease
- 6Disease
- 6Finding of blood, lymphatics and immune system
- 6Hereditary red blood cell disorder
- 7Clinical finding
- 7Disorder of fetus and/or newborn
- 7Hereditary disorder of cellular element of blood
- 8Hereditary disorder by system
- 9Hereditary disease
- 10Genetic disease
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