OMOP Concept 46272743
Eosinophil peroxidase deficiency
StandardConditionSNOMED711160007Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Eosinophil peroxidase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564893 | Presentey Anomaly | Non-standard |
Synonyms
Alternative names recorded for Eosinophil peroxidase deficiency across source vocabularies.
- deficiencia de eosinófilo peroxidasa
- deficiencia de eosinófilo peroxidasa (trastorno)
- deficiencia de peroxidasa eosinofílica
- deficiencia de peroxidasa y fosfolípidos en los eosinófilos
- Eosinophil peroxidase deficiency (disorder)
- Peroxidase and phospholipid deficiency in eosinophils
- Presentey anomaly
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Non-malignant white cell disorder
- 2Autosomal hereditary disorder
- 2White blood cell disorder
- 3Disorder of cellular component of blood
- 3Disorder of immune function
- 3Hereditary disease
- 3OMOP Neutropenia 1
- 4Disease
- 4Finding of blood, lymphatics and immune system
- 4Genetic disease
- 5Clinical finding
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