OMOP Concept 4052693
Iodotyrosyl coupling defect
StandardConditionSNOMED23536000Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Iodotyrosyl coupling defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136548 | Iodotyrosyl Coupling Defect | Non-standard |
| MeSH | C562769 | Thyroid Dyshormonogenesis 3 | Non-standard |
| Nebraska Lexicon | 23536000 | Congenital thyroid hormone coupling defect | Non-standard |
Synonyms
Alternative names recorded for Iodotyrosyl coupling defect across source vocabularies.
- Congenital thyroid hormone coupling defect
- defecto de acoplamiento congénito de hormona tiroidea
- defecto de acoplamiento de hormona tiroidea
- defecto de acoplamiento de yodotirosilo
- defecto de acoplamiento de yodotirosilo (trastorno)
- defecto genético de la hormonogénesis tiroidea tipo III
- GDTH III - genetic defect in thyroid hormonogenesis III
- Genetic defect in thyroid hormonogenesis III
- hipotiroidismo debido a defecto de acoplamiento
- Hypothyroidism due to coupling defect
- Iodotyrosyl coupling defect (disorder)
- Thyroid hormone coupling defect
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Dyshormonogenic goiter
- 1Inherited disorder of thyroid metabolism
- 2Congenital hypothyroidism
- 2Disorder of thyroid gland
- 2Goiter
- 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
- 3Hypothyroidism
- 3Viscus structure finding
- 4Clinical finding
- 4Disease
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Finding of neck region
- 4Hereditary disease
- 4Metabolic disease
- 5Genetic disease
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