OMOP Concept 22281
Sickle cell-hemoglobin SS disease
StandardConditionSNOMED127040003Disorder
Maps from
15
Descendants
11
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Sickle cell-hemoglobin SS disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIM10 | D57 | Sickle-cell disorders | Non-standard |
| HemOnc | 665 | Sickle cell anemia | Non-standard |
| ICD10 | D57 | Sickle-cell disorders | Non-standard |
| ICD10CM | D57 | Sickle-cell disorders | Non-standard |
| ICD10CM | D57.01 | Hb-SS disease with acute chest syndrome | Non-standard |
| ICD10CM | D57.04 | Hb-SS disease with dactylitis | Non-standard |
| ICD10CN | D57 | Sickle-cell disorders | Non-standard |
| ICD10GM | D57 | Sickle-cell disorders | Non-standard |
| KCD7 | D57 | Sickle-cell disorders | Non-standard |
| MeSH | D000755 | Anemia, Sickle Cell | Non-standard |
| Nebraska Lexicon | 127040003 | Sickle cell-haemoglobin SS disease | Non-standard |
| OXMIS | 2825B | ANAEMIA SICKLE CELL | Non-standard |
| Read | D106.00 | Sickle-cell anaemia | Non-standard |
| Read | D106000 | Sickle-cell anaemia of unspecified type | Non-standard |
| Read | D106z00 | Sickle-cell anaemia NOS | Non-standard |
Synonyms
Alternative names recorded for Sickle cell-hemoglobin SS disease across source vocabularies.
- anemia de células falciformes
- anemia drepanocítica
- drepanocitemia
- Drepanocythaemia
- Drepanocythemia
- enfermedad de células falciformes
- enfermedad de la hemoglobina SS-células falciformes
- enfermedad de la hemoglobina SS-células falciformes (trastorno)
- enfermedad por hemoglobina S-S
- Haemoglobin S disease
- Haemoglobin S-S disease
- Hb S disease
- Hb SS disease
- hemoglobinopatía hereditaria homocigótica por hemoglobina S
- Hemoglobin S disease
- Hemoglobin S-S disease
- Hereditary haemoglobinopathy disorder homozygous for haemoglobin S
- Hereditary hemoglobinopathy disorder homozygous for hemoglobin S
- Sickle cell anaemia
- Sickle cell anemia
- Sickle cell-haemoglobin SS disease
- Sickle cell-hemoglobin SS disease (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Anemia due to disturbance of hemoglobin synthesis
- 1Anemia due to intrinsic red cell abnormality
- 1Homozygous hemoglobinopathy
- 1Sickling disorder due to hemoglobin S
- 2Anemia
- 2Hemoglobin below reference range
- 2Hereditary hemoglobinopathy
- 2Hereditary hemoglobin S
- 3Congenital disease
- 3Disorder of cellular component of blood
- 3Hemoglobin level outside reference range
- 3Hemoglobinopathy
- 3Hereditary hemoglobinopathy due to globin chain mutation
- 3Hereditary red blood cell disorder
- 3Measurement finding below reference range
- 4Disease
- 4Disorder of fetus and/or newborn
- 4Finding of blood, lymphatics and immune system
- 4Hematology test outside reference range
- 4Hemoglobin finding
- 4Hereditary disorder of cellular element of blood
- 4Measurement finding outside reference range
- 4Red blood cell disorder
- 5Clinical finding
- 5Disorder of body system
Narrower concepts
(11)Included automatically when you query with descendants.
- 1Hemoglobin SS disease with crisis
- 1Hemoglobin SS disease without crisis
- 1Sickle cell anemia in mother complicating childbirth
- 1Sickle cell anemia with coexistent alpha-thalassemia
- 1Sickle cell anemia with high hemoglobin F
- 2Acute sickle cell splenic sequestration crisis
- 2Hemoglobin SS disease with vasoocclusive crisis
- 2Sickle cell crisis with extensive hemolysis
- 2Vasoocclusive sickle cell crisis
- 3Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis
- 3Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis
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