LP56766-6
Congenital hypothyroidism
Active
Description
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. Source: National Library of Medicine, MeSH 2006
Basic Part Properties
- Name
- Congenital hypothyroidism
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2006-09-01
- Construct for LOINC Short Name
- CH
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- CodeSystem lookup
- https:
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Language Variants
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | 先天性甲状腺机能减退 Synonyms: |
| fr-CA | French (Canada) | Hypothyroïdie congénitale |
| et-EE | Estonian (Estonia) | Kaasasündinud hüpotüreoidism |
| es-ES | Spanish (Spain) | Hipotiroidismo Congenito |
| it-IT | Italian (Italy) | Ipotiroidismo congenito |
| tr-TR | Turkish (Turkey) | Konjenital hipotiroizm |
| ru-RU | Russian (Russian Federation) | Врождённый гипотиреоидизм |
| nl-NL | Dutch (Netherlands) | congenitale hypothyreoïdie |
| fr-BE | French (Belgium) | Hypothyroïdie congénitale |
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