OMOP Concept 4144956
Hereditary spherocytosis due to deficiency of protein 4.2
StandardConditionSNOMED33905008Disorder
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 spherocytosis due to deficiency of protein 4.2 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138733 | Hereditary Spherocytosis due to Deficiency of Protein 4.2 | Non-standard |
Synonyms
Alternative names recorded for Hereditary spherocytosis due to deficiency of protein 4.2 across source vocabularies.
- esferocitosis hereditaria por deficiencia de proteína 4, 2
- esferocitosis hereditaria por deficiencia de proteína 4, 2 (trastorno)
- Hereditary spherocytosis due to deficiency of protein 4.2 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Disorder of hematopoietic structure
- 1Hereditary spherocytosis
- 2Anemia due to membrane defect
- 2Autosomal hereditary disorder
- 2Disorder of body system
- 2Erythrocyte membrane abnormality
- 2Hereditary hemolytic anemia
- 3Anemia due to intrinsic red cell abnormality
- 3Disease
- 3Hemoglobin below reference range
- 3Hemolytic anemia
- 3Hereditary disease
- 3Hereditary red blood cell disorder
- 3Red blood cell disorder
- 4Anemia
- 4Clinical finding
- 4Disorder of cellular component of blood
- 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
- 5Cytopenia
- 5Finding of blood, lymphatics and immune system
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