OMOP Concept 4093515
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
StandardConditionSNOMED24975009Disorder
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 Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134153 | Mild Hereditary Spherocytosis due to Combined Deficiency of Spectrin and Ankyrin | Non-standard |
Synonyms
Alternative names recorded for Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin across source vocabularies.
- esferocitosis hereditaria leve por deficiencia combinada de espectrina Y anquirina
- esferocitosis hereditaria leve por deficiencia combinada de espectrina Y anquirina (trastorno)
- Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (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 spherocytosis due to combined deficiency of spectrin AND ankyrin
- 1Mild hereditary spherocytosis due to spectrin deficiency
- 2Hereditary spherocytosis due to spectrin deficiency
- 3Disorder of hematopoietic structure
- 3Hereditary spherocytosis
- 4Anemia due to membrane defect
- 4Autosomal hereditary disorder
- 4Disorder of body system
- 4Erythrocyte membrane abnormality
- 4Hereditary hemolytic anemia
- 5Anemia due to intrinsic red cell abnormality
- 5Disease
- 5Hemoglobin below reference range
- 5Hemolytic anemia
- 5Hereditary disease
- 5Hereditary red blood cell disorder
- 5Red blood cell disorder
- 6Anemia
- 6Clinical finding
- 6Disorder of cellular component of blood
- 6Genetic disease
- 6Hemoglobin level outside reference range
- 6Hemolytic disorder
- 6Hereditary disorder of cellular element of blood
- 6Measurement finding below reference range
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