OMOP Concept 4217606
Iodide peroxidase defect
StandardConditionSNOMED81873006Disorder
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 Iodide peroxidase defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136558 | Iodide Peroxidase Defect | Non-standard |
| Nebraska Lexicon | 81873006 | Defective iodide peroxidase activity | Non-standard |
Synonyms
Alternative names recorded for Iodide peroxidase defect across source vocabularies.
- actividad deficiente de la yoduro peroxidasa
- Defective iodide peroxidase activity
- defecto de yoduro peroxidasa
- defecto de yoduro peroxidasa (trastorno)
- Iodide peroxidase defect (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Inherited disorder of thyroid metabolism
- 2Disorder of thyroid gland
- 2Hereditary disorder of endocrine system
- 2Inborn error of metabolism
- 3Congenital disease
- 3Disorder of endocrine system
- 3Disorder of neck
- 3Finding of thyroid gland
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 4Disease
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Finding of neck region
- 4Hereditary disease
- 4Metabolic disease
- 5Clinical finding
- 5Genetic disease
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