OMOP Concept 4125633
Hereditary elliptocytosis with transient poikilocytosis
StandardConditionSNOMED234410008Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary elliptocytosis with transient poikilocytosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234410008 | Hereditary elliptocytosis with transient poikilocytosis | Non-standard |
Synonyms
Alternative names recorded for Hereditary elliptocytosis with transient poikilocytosis across source vocabularies.
- eliptocitosis hereditaria con poiquilocitosis transitoria
- eliptocitosis hereditaria con poiquilocitosis transitoria (trastorno)
- Hereditary elliptocytosis with transient poikilocytosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(44)Roll up to these when you need a wider cohort.
- 1Hereditary elliptocytosis
- 2Congenital hemolytic anemia
- 2Congenital malformation
- 2Developmental hereditary disorder
- 2Erythrocyte membrane abnormality
- 2Hereditary hemolytic anemia
- 3Congenital anemia
- 3Congenital disease
- 3Developmental disorder
- 3Hemoglobin below reference range
- 3Hemolytic anemia
- 3Hereditary disease
- 3Hereditary red blood cell disorder
- 3Red blood cell disorder
- 4Anemia
- 4Disease
- 4Disorder of body system
- 4Disorder of cellular component of blood
- 4Disorder of fetus and/or newborn
- 4Genetic disease
- 4Hemoglobin level outside reference range
- 4Hemolytic disorder
- 4Hereditary disorder of cellular element of blood
- 4Measurement finding below reference range
- 4Red blood cell count below reference range
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