OMOP Concept 4213628
Sickling disorder due to hemoglobin S
StandardConditionSNOMED417357006Disorder
Maps from
16
Descendants
34
Valid from
31 Jul 2005
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
16 source codes normalize to Sickling disorder due to hemoglobin S via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117703 | Sickle-cell anemia | Non-standard |
| CIEL | 158813 | Sickling disorder due to hemoglobin S | Non-standard |
| CIM10 | D57.8 | Other sickle-cell disorders | Non-standard |
| ICD10 | D57.8 | Other sickle-cell disorders | Non-standard |
| ICD10CM | D57.8 | Other sickle-cell disorders | Non-standard |
| ICD10CM | D57.813 | Other sickle-cell disorders with cerebral vascular involvement | Non-standard |
| ICD10CM | D57.814 | Other sickle-cell disorders with dactylitis | Non-standard |
| ICD10CN | D57.8 | Other sickle-cell disorders | Non-standard |
| ICD10CN | D57.800 | Other sickle-cell disorders | Non-standard |
| ICD10GM | D57.8 | Other sickle-cell disorders | Non-standard |
| ICD9CM | 282.6 | Sickle-cell disease | Non-standard |
| ICD9CM | 282.60 | Sickle-cell disease, unspecified | Non-standard |
| KCD7 | D57.8 | Other sickle-cell disorders | Non-standard |
| Nebraska Lexicon | 417357006 | Sickle cell syndrome | Non-standard |
| Read | Dyu1200 | [X]Other sickle-cell disorders | Non-standard |
| UK Biobank | 6-1339 | sickle cell disease | Non-standard |
Synonyms
Alternative names recorded for Sickling disorder due to hemoglobin S across source vocabularies.
- drepanocitosis por hemoglobina S
- drepanocitosis por hemoglobina S (trastorno)
- Sickle cell disease
- Sickle cell syndrome
- Sickling disorder due to haemoglobin S
- Sickling disorder due to hemoglobin S (disorder)
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 hemoglobin S
- 2Hereditary hemoglobinopathy due to globin chain mutation
- 3Hereditary hemoglobinopathy
- 4Congenital disease
- 4Hemoglobinopathy
- 4Hereditary red blood cell disorder
- 5Disorder of fetus and/or newborn
- 5Hereditary disorder of cellular element of blood
- 5Red blood cell disorder
- 6Disease
- 6Disorder of body system
- 6Disorder of cellular component of blood
- 6Hereditary disorder by system
- 7Clinical finding
- 7Finding of blood, lymphatics and immune system
- 7Hereditary disease
- 8Genetic disease
Narrower concepts
(34)Included automatically when you query with descendants.
- 1Double heterozygous sickling disorder
- 1Hemoglobin S sickling disorder with crisis
- 1Hemoglobin S sickling disorder without crisis
- 1Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome
- 1Sickle cell-hemoglobin SS disease
- 1Sickle cell-thalassemia disease
- 2Hemoglobin SS disease with crisis
- 2Hemoglobin SS disease without crisis
- 2Sickle cell anemia in mother complicating childbirth
- 2Sickle cell anemia with coexistent alpha-thalassemia
- 2Sickle cell anemia with high hemoglobin F
- 2Sickle cell-beta-thalassemia
- 2Sickle cell-hemoglobin C disease
- 2Sickle cell-hemoglobin C disease with crisis
- 2Sickle cell-hemoglobin C disease without crisis
- 2Sickle cell-hemoglobin D disease
- 2Sickle cell-hemoglobin D disease with crisis
- 2Sickle cell-hemoglobin D disease without crisis
- 2Sickle cell-hemoglobin E disease
- 2Sickle cell-hemoglobin E disease with crisis
- 2Sickle cell-hemoglobin E disease without crisis
- 2Sickle cell-hemoglobin Lepore disease
- 2Sickle cell-Hemoglobin O Arab disease
- 2Sickle cell-thalassemia disease with crisis
- 2Sickle cell-thalassemia disease without crisis
- 3Acute sickle cell splenic sequestration crisis
- 3Hemoglobin SS disease with vasoocclusive crisis
- 3Sickle cell-beta0-thalassemia
- 3Sickle cell beta plus thalassemia
- 3Sickle cell crisis with extensive hemolysis
- 3Sickle cell-delta beta0-thalassemia
- 3Vasoocclusive sickle cell crisis
- 4Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis
- 4Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis
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