OMOP Concept 4243676
Hereditary elliptocytosis due to deficiency of protein 4.1
StandardConditionSNOMED5994005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Hereditary elliptocytosis due to deficiency of protein 4.1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138781 | Hereditary Elliptocytosis due to Deficiency of Protein 4.1 | Non-standard |
| Nebraska Lexicon | 5994005 | Hereditary elliptocytosis due to deficiency of protein 4.1 | Non-standard |
Synonyms
Alternative names recorded for Hereditary elliptocytosis due to deficiency of protein 4.1 across source vocabularies.
- eliptocitosis hereditaria por deficiencia de proteína 4, 1
- eliptocitosis hereditaria por deficiencia de proteína 4, 1 (trastorno)
- Hereditary elliptocytosis due to deficiency of protein 4.1 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(47)Roll up to these when you need a wider cohort.
- 1Anemia due to intrinsic red cell abnormality
- 1Autosomal dominant hereditary disorder
- 1Hereditary elliptocytosis
- 2Anemia
- 2Autosomal hereditary disorder
- 2Congenital hemolytic anemia
- 2Congenital malformation
- 2Developmental hereditary disorder
- 2Erythrocyte membrane abnormality
- 2Hereditary hemolytic anemia
- 3Congenital anemia
- 3Congenital disease
- 3Developmental disorder
- 3Disorder of cellular component of blood
- 3Hemoglobin below reference range
- 3Hemolytic anemia
- 3Hereditary disease
- 3Hereditary red blood cell disorder
- 3Red blood cell disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Finding of blood, lymphatics and immune system
- 4Genetic disease
- 4Hemoglobin level outside reference range
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