OMOP Concept 22288
Hereditary elliptocytosis
StandardConditionSNOMED191169008Disorder
Maps from
16
Descendants
9
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 Hereditary elliptocytosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138786 | Hereditary elliptocytosis | Non-standard |
| CIEL | 143979 | Congenital elliptocytosis | Non-standard |
| CIM10 | D58.1 | Hereditary elliptocytosis | Non-standard |
| ICD10 | D58.1 | Hereditary elliptocytosis | Non-standard |
| ICD10CM | D58.1 | Hereditary elliptocytosis | Non-standard |
| ICD10CN | D58.1 | Hereditary elliptocytosis | Non-standard |
| ICD10CN | D58.100 | Hereditary elliptocytosis | Non-standard |
| ICD10CN | D58.101 | Congenital oval cell anemia (machine translation) | Non-standard |
| ICD10GM | D58.1 | Hereditary elliptocytosis | Non-standard |
| ICD9CM | 282.1 | Hereditary elliptocytosis | Non-standard |
| KCD7 | D58.1 | Hereditary elliptocytosis | Non-standard |
| MeSH | D004612 | Elliptocytosis, Hereditary | Non-standard |
| Nebraska Lexicon | 178935009 | Congenital elliptocytosis | Non-standard |
| Nebraska Lexicon | 191169008 | Hereditary elliptocytosis | Non-standard |
| Read | D101.00 | Hereditary elliptocytosis | Non-standard |
| Read | D101.11 | Ovalocytosis - hereditary | Non-standard |
Synonyms
Alternative names recorded for Hereditary elliptocytosis across source vocabularies.
- Congenital elliptocytosis
- eliptocitosis congénita
- eliptocitosis hereditaria
- eliptocitosis hereditaria (trastorno)
- HE - Hereditary elliptocytosis
- Hereditary elliptocytosis (disorder)
- Hereditary ovalocytosis
- ovalocitosis hereditaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Congenital hemolytic anemia
- 1Congenital malformation
- 1Developmental hereditary disorder
- 1Erythrocyte membrane abnormality
- 1Hereditary hemolytic anemia
- 2Congenital anemia
- 2Congenital disease
- 2Developmental disorder
- 2Hemoglobin below reference range
- 2Hemolytic anemia
- 2Hereditary disease
- 2Hereditary red blood cell disorder
- 2Red blood cell disorder
- 3Anemia
- 3Disease
- 3Disorder of body system
- 3Disorder of cellular component of blood
- 3Disorder of fetus and/or newborn
- 3Genetic disease
- 3Hemoglobin level outside reference range
- 3Hemolytic disorder
- 3Hereditary disorder of cellular element of blood
- 3Measurement finding below reference range
- 3Red blood cell count below reference range
- 4Clinical finding
Narrower concepts
(9)Included automatically when you query with descendants.
- 1Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 1Hereditary elliptocytosis due to abnormal protein 4.1
- 1Hereditary elliptocytosis due to alpha spectrin defect
- 1Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
- 1Hereditary elliptocytosis due to beta spectrin defect in self-association
- 1Hereditary elliptocytosis due to deficiency of protein 4.1
- 1Hereditary elliptocytosis due to glycophorin C deficiency
- 1Hereditary elliptocytosis with transient poikilocytosis
- 1Homozygous hereditary elliptocytosis
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