OMOP Concept 24006
Sickle cell-hemoglobin C disease
StandardConditionSNOMED35434009Disorder
Maps from
16
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
16 source codes normalize to Sickle cell-hemoglobin C disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 112975 | Sickle-cell/Hb-C disease without crisis | Non-standard |
| CIEL | 168107 | Haemoglobin SC genotype | Non-standard |
| CIM10 | D57.2 | Double heterozygous sickling disorders | Non-standard |
| ICD10 | D57.2 | Double heterozygous sickling disorders | Non-standard |
| ICD10CM | D57.2 | Sickle-cell/Hb-C disease | Non-standard |
| ICD10CM | D57.214 | Sickle-cell/Hb-C disease with dactylitis | Non-standard |
| ICD10CN | D57.2 | Double heterozygous sickling disorders | Non-standard |
| ICD10CN | D57.200 | Double heterozygous sickling disorders | Non-standard |
| ICD10CN | D57.201 | Hemoglobin -SC disease (machine translation) | Non-standard |
| ICD10CN | D57.202 | Hemoglobin -SD disease (machine translation) | Non-standard |
| ICD10CN | D57.203 | Hemoglobin -SE disease (machine translation) | Non-standard |
| ICD10GM | D57.2 | Double heterozygous sickling disorders | Non-standard |
| KCD7 | D57.2 | Double heterozygous sicking disorders | Non-standard |
| MeSH | D006450 | Hemoglobin SC Disease | Non-standard |
| Nebraska Lexicon | 35434009 | Sickle C disease | Non-standard |
| Read | D106300 | Sickle-cell anaemia with haemoglobin C disease | Non-standard |
Synonyms
Alternative names recorded for Sickle cell-hemoglobin C disease across source vocabularies.
- Double heterozygous for Hb S and Hb D
- enfermedad de células falciformes - hemoglobina C
- enfermedad de células falciformes - hemoglobina C (trastorno)
- enfermedad por HbS - HbC
- enfermedad por hemoglobina S - C
- Haemoglobin S-C disease
- Haemoglobin S/C disease
- Hb SC disease
- HbS-HbC disease
- Hemoglobin S-C disease
- Hemoglobin S/C disease
- Sickle cell anaemia with haemoglobin C disease
- Sickle cell anemia with hemoglobin C disease
- Sickle cell haemoglobin C
- Sickle cell-haemoglobin C disease
- Sickle cell hemoglobin C
- Sickle cell-hemoglobin C disease (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Double heterozygous sickling disorder
- 1Mixed hemoglobin disorder
- 2Hemoglobinopathy
- 2Sickling disorder due to hemoglobin S
- 3Hereditary hemoglobin S
- 3Red blood cell disorder
- 4Disorder of body system
- 4Disorder of cellular component of blood
- 4Hereditary hemoglobinopathy due to globin chain mutation
- 5Disease
- 5Finding of blood, lymphatics and immune system
- 5Hereditary hemoglobinopathy
- 6Clinical finding
- 6Congenital disease
- 6Hereditary red blood cell disorder
- 7Disorder of fetus and/or newborn
- 7Hereditary disorder of cellular element of blood
- 8Hereditary disorder by system
- 9Hereditary disease
- 10Genetic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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