LOINC
Version 2.73

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