OMOP Concept 25518
Sickle cell trait
StandardConditionSNOMED16402000Disorder
Maps from
14
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
14 source codes normalize to Sickle cell trait via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 126513 | Sickle cell trait | Non-standard |
| CIEL | 1627 | Personal history of sickle cell trait | Non-standard |
| CIM10 | D57.3 | Sickle-cell trait | Non-standard |
| ICD10 | D57.3 | Sickle-cell trait | Non-standard |
| ICD10CM | D57.3 | Sickle-cell trait | Non-standard |
| ICD10CN | D57.3 | Sickle-cell trait | Non-standard |
| ICD10CN | D57.300 | Sickle-cell trait | Non-standard |
| ICD10CN | D57.301 | Disease hybrid hemoglobin S (machine translation) | Non-standard |
| ICD10GM | D57.3 | Sickle-cell trait | Non-standard |
| ICD9CM | 282.5 | Sickle-cell trait | Non-standard |
| KCD7 | D57.3 | Sickle-cell trait | Non-standard |
| MeSH | D012805 | Sickle Cell Trait | Non-standard |
| Nebraska Lexicon | 16402000 | Sickle cells present | Non-standard |
| Read | D105.00 | Sickle-cell trait | Non-standard |
Synonyms
Alternative names recorded for Sickle cell trait across source vocabularies.
- AS - Sickle cell trait
- Drepanocytosis
- genotipo de hemoglobina A - S
- Haemoglobin A-S genotype
- Haemoglobin S-A disorder
- Haemoglobin S trait
- Hemoglobin A-S genotype
- hemoglobina S heterocigota
- Hemoglobin S-A disorder
- Hemoglobin S trait
- Heterozygous for Hb S
- Heterozygous haemoglobin S
- Heterozygous hemoglobin S
- rasgo de drepanocitosis
- rasgo de drepanocitosis (trastorno)
- rasgo de hemoglobina S
- RBC's - sickle cells present
- Sickle cells present
- Sickle cell trait (disorder)
- trastorno de hemoglobina S - A
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Hereditary hemoglobin S
- 1Heterozygous hemoglobinopathy
- 2Hereditary hemoglobinopathy
- 2Hereditary hemoglobinopathy due to globin chain mutation
- 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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