Version 2.78

Term Description

Used to order tests that assist in the risk calculations for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 (Down's Syndrome) and Trisomy 18 (Edward's syndrome).. Analytes could be Alpha-1-fetoprotein, Choriogonadotropin, Estriol.unconjugated, Inhibin A, Pregnancy associated plasma protein A and/or Nuchal translucency.
Source: Regenstrief LOINC

Panel Hierarchy

Details for each LOINC in Panel LHC-Forms

Fully-Specified Name

Component
Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel
Property
-
Time
Pt
System
Ser/Plas
Scale
-
Method

Additional Names

Short Name
Mat scn for fetal abnormalities SerPl
Display Name
Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel
Consumer Name Alpha Get Info
Maternal screen for fetal Abnormalities such As open neural tube Defects, trisomy 21 or trisomy 18 panel, Blood

Basic Attributes

Class
PANEL.CHEM
Type
Laboratory
First Released
Version 2.22
Last Updated
Version 2.73
Order vs. Observation
Order
Common Test Rank Get Info
5338
Panel Type
Panel

Language Variants Get Info

Tag Language Translation
es-ES Spanish (Spain) Screenin materno para detectar anormalidades fetales como defectos abiertos del tubo neural, trisomía 21 o trisomía 18:Propiedades mixtas (sólo paneles):Punto temporal:Suero o Plasma:-:
es-MX Spanish (Mexico) Detección materna de anomalías fetales como defectos del tubo neural abierto, panel de trisomía 21 o trisomía 18:-:Punto temporal:Suero o Plasma:-:
et-EE Estonian (Estonia) Sünnieelne kromosoomihaiguste riskihinnang (avatud neuraaltoru, trisoomia 21, trisoomia 18):-:Pt:S/P:-:
Synonyms: Juhuslik Plasma Seerum Seerum või plasma
fr-FR French (France) Dépistage maternel des anomalies fœtales comme l'ouverture du tube neural, trisomie 21 ou 18 panel:-:Ponctuel:Sérum/Plasma:-:
fr-BE French (Belgium) Screening maternel anomalies foetales. Panel NTD &Spina bifida,Trisomie 21 et 18:-:Temps ponctuel:Sérum/Plasma:-:
it-IT Italian (Italy) Screening materno per anomalie fetali come Difetti Aperti del Tubo Neurale, Trisomia 21 o Trisomia 18, panel:-:Pt:Siero/Plasma:-:
Synonyms: Chimica Panel screening materno per anomalie fetali come D Plasma Punto nel tempo (episodio) Set di prescrizione chimica Siero Siero o Plasma
nl-NL Dutch (Netherlands) maternale screening op foetale afwijkingen zoals open neuraalbuisdefecten, trisomie 21 of trisomie 18 panel:-:moment:serum of plasma:-:
pt-BR Portuguese (Brazil) Maternal tela de anomalias fetais, como Defeitos de abertura do Tubo Neural, Trissomia 21 ou Trissomia 18 painel:-:Pt:Sor/Plas:-:
Synonyms: ; Mat scn for fetalAbnormalities; Point in time; Random; SerPl; SerPlas; SerP; Serum; SR; Plasma; Pl; Plsm; Scr; Scn; Scrn; Down syndrome; Edward syndrome; Ts; Pnl; Pan; Panl; Arterial Stenosis; PANEL.CHEMISTRY; PANEL.CHEMISTRY; Chemistry
ru-RU Russian (Russian Federation) Мать скрин на плод аномалии, такие как Открытая Невральная Трубка Дефекты, Трисомия 21 или Трисомия 18 панель:-:ТчкВрм:Сыв/Плаз:-:
Synonyms: Плазма Сыворотка Сыворотка или Плазма Точка во времени;Момент Трисомия 21 в анамнезе
zh-CN Chinese (China) 针对开放型神经管缺陷、三体型 21 或三体型 18 之类胎儿异常的母亲筛查试验组套:-:时间点:血清/血浆:-:
Synonyms: 21 三体型综合征（唐氏综合征、Down 氏综合征、Down 综合征、21 三体性、21 号染色体三体型、21 号染色体三体性） 三体型 三体细胞 三染色体性 三染色体细胞 动脉狭窄 动脉狭窄（Arterial Stenosis，AS） 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 医嘱套餐 医嘱套餐类 医嘱套餐组 医嘱组 医嘱组.化学试验;化学组套（组合、医嘱组、套餐、套餐医嘱、医嘱套餐、组合申请、组合项目）;化学医嘱组类;医嘱组.化学;医嘱组.化学检验项目;医嘱组类.化学;医嘱组类.化学检验项目;医嘱组类.化学试验;实验室医嘱组类.化学;实验室医嘱组类.化学检验项目;实验室医嘱组类.化学试验 医嘱组合 医嘱组合类 医嘱组套 医嘱组套类 医嘱组类 多重;多重型;多重标尺类型;多重精度类型 套餐 套餐医嘱 套餐医嘱组 套餐医嘱组类 实验室医嘱套餐 实验室医嘱套餐类 实验室医嘱组 实验室医嘱组合类 实验室医嘱组套 实验室医嘱组套类 实验室套餐医嘱组 实验室套餐医嘱组类 实验室检验项目医嘱组合类 实验室检验项目组合类 时刻;随机;随意;瞬间 检验医嘱组合类 检验项目医嘱组合类 检验项目组合类 筛查 筛查试验 筛选试验 组 组合 组合医嘱 组合类 组套 血清或血浆 过筛 过筛试验 针对开放型神经管缺陷、三体型 21 或三体型 18 之类胎儿异常的母亲筛查试验组套（组合、医嘱组、套餐、套餐医嘱、医嘱套餐、组合申请、组合项目）;针对开放型神经管畸形、三体 21 或三体 18 之类胎儿异常的母亲筛查试验医嘱组;针对开放型神经管畸形、三体 21 或三体 18 之类胎儿畸形的母亲筛查试验医嘱组;针对开放型神经管畸形、三体性 21 或三体性 18 之类胎儿异常的母亲筛查试验医嘱组;针对开放型神经管畸形、三体性 21 或三体性 18 之类胎儿畸形的母亲筛查试验医嘱组;针对开放型神经管缺损、三体

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=50580-0