OMOP Concept 4138560
Mild hereditary spherocytosis due to spectrin deficiency
StandardConditionSNOMED32648007Disorder
Maps from
2
Descendants
1
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 Mild hereditary spherocytosis due to spectrin deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134152 | Mild Hereditary Spherocytosis due to Spectrin Deficiency | Non-standard |
| Nebraska Lexicon | 32648007 | Mild hereditary spherocytosis due to spectrin deficiency | Non-standard |
Synonyms
Alternative names recorded for Mild hereditary spherocytosis due to spectrin deficiency across source vocabularies.
- esferocitosis hereditaria leve por deficiencia de espectrina
- esferocitosis hereditaria leve por deficiencia de espectrina (trastorno)
- Mild hereditary spherocytosis due to spectrin deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Hereditary spherocytosis due to spectrin deficiency
- 2Disorder of hematopoietic structure
- 2Hereditary spherocytosis
- 3Anemia due to membrane defect
- 3Autosomal hereditary disorder
- 3Disorder of body system
- 3Erythrocyte membrane abnormality
- 3Hereditary hemolytic anemia
- 4Anemia due to intrinsic red cell abnormality
- 4Disease
- 4Hemoglobin below reference range
- 4Hemolytic anemia
- 4Hereditary disease
- 4Hereditary red blood cell disorder
- 4Red blood cell disorder
- 5Anemia
- 5Clinical finding
- 5Disorder of cellular component of blood
- 5Genetic disease
- 5Hemoglobin level outside reference range
- 5Hemolytic disorder
- 5Hereditary disorder of cellular element of blood
- 5Measurement finding below reference range
- 5Red blood cell count below reference range
- 6Cytopenia
Narrower concepts
(1)Included automatically when you query with descendants.
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