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Part 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

LOINC Names Get Info

Fully-Specified Name
Congenital hypothyroidism:Imp:Pt:Bld.dot:Nom:
Long Common Name
Congenital hypothyroidism newborn screen interpretation
Short Name
CH DBS-Imp
Display Name
Congenital hypothyroidism (DBS) [Interp]
Consumer Name Alpha Get Info
Congenital hypothyroidism, Dried blood spot

Part Model Get Info

  • Component
    Congenital hypothyroidism
    LP56766-6
    • Analyte
      Congenital hypothyroidism
      LP56766-6
      • Component Numerator
        Congenital hypothyroidism
        LP56766-6
        • Component Numerator Core
          Congenital hypothyroidism
          LP56766-6
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Imp
    LP6819-9
  • Time
    Pt
    LP6960-1
  • System
    Bld.dot
    LP21304-8
    • System Core
      Bld.dot
      LP21304-8
    • Super System
      NULL
       
  • Scale
    Nom
    LP7750-5
  • Method
    NULL
     

Preferred Answer List: LL6931-1

AnswerCodeScoreAnswer ID
BorderlineLA4259-3
IndeterminateCopyright http://snomed.info/sct ID:82334004 Indeterminate (qualifier value)LA11884-6
One or more tests pendingLA16204-2
Screen NegativeLA34518-3
Screen PositiveLA34519-1
Specimen unacceptable for at least one conditionLA34520-9
InconclusiveCopyright http://snomed.info/sct ID:419984006 Inconclusive (qualifier value)LA9663-1
Not testedLA13538-6

Basic Attributes

Class
CHEM
Type
Laboratory
First Released
Version 2.19
Last Updated
Version 2.73 (MIN)
Change Reason
Release 2.81: AnswerListId: APHL change request; Previous Releases: Changed answer list from "Normative" to "Preferred" to fit the current LOINC model.
Order vs. Observation
Observation
Common Test Rank Get Info
14221

Member of these Panels

LOINCLong Common Name
54076-5Endocrine newborn screening panel
54075-7Endocrine newborn screening panel (SI units)
54089-8Newborn screening panel American Health Information Community (AHIC)
54077-3Thyroid newborn screening panel (SI units)

Member of these Groups Get Info

LOINC GroupGroup Name
LG18377-8Congenital hypothyroidism|Imp|Pt|Bld.dot

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Kongenitální hypotyreóza:Interpretace:Časový bod:Suchá krevní kapka (DBS):Nominální:
el-GRGreek (Greece)Συγγενής υποθυρεοειδισμός:Imp:Pt:Bld.dot:Nom:
Synonyms: Bld.dot CHEM Imp Nom Pt Αίμα Συγγενής υποθυρεοειδισμός
es-ESSpanish (Spain)Hipotiroidismo Congenito:Impresión/interpretación del estudio:Punto temporal:gota de sangre (papel de filtro):Nom:
es-MXSpanish (Mexico)Hipotiroidismo congénito:Impresión / interpretación del estudio:Punto temporal:DBS:Nominal:
fr-CAFrench (Canada)Hypothyroïdie congénitale:Impression:Temps ponctuel:Sang sur papier filtre:Nominal:
fr-FRFrench (France)Hypothyroïdisme congénital:Interprétation:Ponctuel:Sang buvard:Résultat nominal:
fr-BEFrench (Belgium)Hypothyroïdie congénitale:Impression/interprétation d'étude:Temps ponctuel:Sang sur papier filtre:Nominal:
it-ITItalian (Italy)Ipotiroidismo congenito:Imp:Pt:Sangue.su carta da filtro:Nom:
Synonyms: Chimica Impressione/interpretazione di studio Punto nel tempo (episodio) Sangue Spot sangue secco
nl-NLDutch (Netherlands)congenitale hypothyreoïdie:interpretatie:moment:gedroogde bloedspot:nominaal:
pt-BRPortuguese (Brazil)Hipotireoidismo congênito:Imp:Pt:SgPapel:Nom:
Synonyms: ; CH; Interpretation; Interp; Impression; Impressions; Point in time; Random; DBS; Filter paper; FP; Dried blood spot; Blood; WB; Whole blood; Nominal; Chemistry
ru-RURussian (Russian Federation)Врождённый гипотиреоидизм:Впчт:ТчкВрм:Кр.Сух.капл:Ном:
Synonyms: Впечатление/интерпретация исследования Кровь Кровь сухая капля Номинальный;Именной Точка во времени;Момент
tr-TRTurkish (Turkey)Konjenital hipotiroizm:İzlnm:Zmlı:Kan.nokta:Snf:
zh-CNChinese (China)先天性甲状腺机能减退:印象:时间点:全血.斑点:名义型:
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） 全血斑点(滤纸);滤纸;血液.斑点;血液斑点(滤纸) 分类型应答;分类型结果;名义性;名称型;名词型;名词性;标称性;没有自然次序的名义型或分类型应答 化学;化学检验项目;化学检验项目类;化学类;化学试验;非刺激耐受型化学检验项目;非刺激耐受型化学检验项目类;非刺激耐受型化学试验;非刺激耐受型化学试验类 印象是一种诊断陈述，始终是对其他某种观察指标的解释或抽象（一系列检验项目结果、一幅图像或者整个某位病人），而且几乎总是由某位专业人员产生。;检查印象;检查印象/解释;检查的印象/解释;检查解释;解释;阐释 时刻;随机;随意;瞬间 甲状腺功能减退;甲减;甲状腺功能低下症;甲状腺功能减退症 血;血液

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=46762-1