LOINC
Version 2.73

46762-1Congenital hypothyroidism newborn screen interpretationActive

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

Fully-Specified Name

Component
Congenital hypothyroidism
Property
Imp
Time
Pt
System
Bld.dot
Scale
Nom
Method

Additional Names

Short Name
CH DBS-Imp
Display Name
Congenital hypothyroidism (DBS) [Interp]
Consumer Name Alpha
Congenital hypothyroidism, Dried blood spot

Preferred Answer List LL840-0

Source: Regenstrief Institute

Answer Code Score Answer ID
In range LA18592-8
Borderline LA4259-3
Indeterminate Copyright http://snomed.info/sct ID:82334004 Indeterminate (qualifier value) LA11884-6
Out of range LA18593-6
Out of range requiring further dried blood spot testing for at least one condition LA12430-7
Out of range requiring immediate referral LA25817-0
Out of range requiring immediate second-tier testing for at least one condition LA12431-5
Out of range requiring deferred follow-up for at least one condition LA18594-4
One or more tests pending LA16204-2
Specimen unsatisfactory for at least one condition LA16205-9

Basic Attributes

Class
CHEM
Type
Laboratory
First Released
Version 2.19
Last Updated
Version 2.73
Change Reason
Changed answer list from "Normative" to "Preferred" to fit the current LOINC model.
Order vs. Observation
Observation
Common US Lab Results Rank
14221

Member of these Panels

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

Member of these Groups

LG18377-8 Congenital hypothyroidism|Imp|Pt|Bld.dot

Language Variants Get Info

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:
nl-NLDutch (Netherlands)
congenitale hypothyreoïdie:interpretatie:moment:gedroogde bloedspot:nominaal:
fr-BEFrench (Belgium)
Hypothyroïdie congénitale:Impression/interprétation d'étude:Temps ponctuel:Sang sur papier filtre:Nominal:
fr-CAFrench (Canada)
Hypothyroïdie congénitale:Impression/interprétation d'étude:Temps ponctuel:Sang sur papier filtre:Nominal:
fr-FRFrench (France)
Hypothyroïdisme congénital:Interprétation:Ponctuel:Sang buvard:Résultat nominal:
it-ITItalian (Italy)
Ipotiroidismo congenito:Imp:Pt:Sangue.su carta da filtro:Nom:
pt-BRPortuguese (Brazil)
Hipotireoidismo congênito:Imp:Pt:SgPapel:Nom:
ru-RURussian (Russian Federation)
Врождённый гипотиреоидизм:Впчт:ТчкВрм:Кр.Сух.капл:Ном:
es-MXSpanish (Mexico)
Hipotiroidismo congénito:Impresión / interpretación del estudio:Punto temporal:DBS:Nominal:
es-ESSpanish (Spain)
Hipotiroidismo Congenito:Impresión/interpretación del estudio:Punto temporal:gota de sangre (papel de filtro):Nom:
tr-TRTurkish (Turkey)
Konjenital hipotiroizm:İzlnm:Zmlı:Kan.nokta:Snf:

LOINC FHIR® API Example - CodeSystem Request Get Info

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