OMOP Concept 4175331
Congenital hemolytic anemia
StandardConditionSNOMED42601008Disorder
Maps from
3
Descendants
11
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Congenital hemolytic anemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143936 | Congenital hemolytic anemia | Non-standard |
| HPO | HP_0004804 | Congenital hemolytic anemia | Non-standard |
| Nebraska Lexicon | 42601008 | Congenital haemolytic anaemia | Non-standard |
Synonyms
Alternative names recorded for Congenital hemolytic anemia across source vocabularies.
- anemia hemolítica congénita
- anemia hemolítica congénita (trastorno)
- Congenital haemolytic anaemia
- Congenital hemolytic anemia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Congenital anemia
- 1Hemolytic anemia
- 1Red blood cell disorder
- 2Anemia
- 2Congenital disease
- 2Disorder of body system
- 2Disorder of cellular component of blood
- 2Hemoglobin below reference range
- 2Hemolytic disorder
- 2Red blood cell count below reference range
- 3Cytopenia
- 3Disease
- 3Disorder of fetus and/or newborn
- 3Finding of blood, lymphatics and immune system
- 3Hemoglobin level outside reference range
- 3Hemolysis
- 3Measurement finding below reference range
- 3Red blood cell count outside reference range
- 4Blood cell count outside reference range
- 4Clinical finding
- 4Hematology test outside reference range
- 4Hemoglobin finding
- 4Measurement finding outside reference range
- 4Red blood cell count - finding
- 4Red blood cell destruction finding
Narrower concepts
(11)Included automatically when you query with descendants.
- 1Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
- 1Hereditary elliptocytosis
- 2Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 2Hereditary elliptocytosis due to abnormal protein 4.1
- 2Hereditary elliptocytosis due to alpha spectrin defect
- 2Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
- 2Hereditary elliptocytosis due to beta spectrin defect in self-association
- 2Hereditary elliptocytosis due to deficiency of protein 4.1
- 2Hereditary elliptocytosis due to glycophorin C deficiency
- 2Hereditary elliptocytosis with transient poikilocytosis
- 2Homozygous hereditary elliptocytosis
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