Version 2.77

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

Part Display Name
Congenital hypothyroidism
Part Type
Component (Describes the core component or analyte measured)
Created On
2006-09-01
Construct for LOINC Short Name
CH

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP56766-6

Language Variants Get Info

Tag Language Translation
zh-CN Chinese (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)
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