LP56766-6Congenital hypothyroidismActive
Description
LP56766-6 Congenital hypothyroidism
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
- Type
- Component
- Created On
- 2006-09-01
- Construct for LOINC Short Name
- CH
LOINC FHIR® API Example - CodeSystem Request Get Info
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP56766-6
Language Variants Get Info
- zh-CNChinese (China)
- 先天性甲状腺机能减退
Synonyms: CH;先天性甲状腺功能低下; 先天性甲状腺机能减退（Congenital Hypothyroidism， CH） - nl-NLDutch (Netherlands)
- congenitale hypothyreoïdie
- et-EEEstonian (Estonia)
- Kaasasündinud hüpotüreoidism
- fr-BEFrench (Belgium)
- Hypothyroïdie congénitale
- fr-CAFrench (Canada)
- Hypothyroïdie congénitale
- it-ITItalian (Italy)
- Ipotiroidismo congenito
- ru-RURussian (Russian Federation)
- Врождённый гипотиреоидизм
- es-ESSpanish (Spain)
- Hipotiroidismo Congenito
Synonyms: CH - tr-TRTurkish (Turkey)
- Konjenital hipotiroizm
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