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Part Description

LP185800-2   Based on maternal age
The fetal risk for having certain disorders, such as Trisomy 21, varies based on maternal age. For such disorders, an individual infant's risk can be estimated based on known population statistics for how many women in a particular age group have an infant born with the condition compared to the total number of pregnancies for that age group. For example, the fetal Trisomy 21 risk is 1 out of 1,000 for a maternal age of 30 and 1 out of 100 for a maternal age of 40. Source: Regenstrief LOINC

LOINC Names Get Info

Fully-Specified Name
Monosomy X prior risk:Likelihood:Pt:^Fetus:Nar:Based on maternal age
Long Common Name
Fetal Monosomy X prior risk [Likelihood] Based on maternal age Narrative
Short Name
Fet Ms X prior risk from Mat age
Display Name
Monosomy X prior risk Based on maternal age Nar (fetus)
Consumer Name Alpha Get Info
Fetal Monosomy X Prior Risk

Part Model Get Info

  • Component
    Monosomy X prior risk
    LP185767-3
    • Analyte
      Monosomy X prior risk
      LP185767-3
      • Component Numerator
        Monosomy X prior risk
        LP185767-3
        • Component Numerator Core
          Monosomy X prior risk
          LP185767-3
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Likelihood
    LP185777-2
  • Time
    Pt
    LP6960-1
  • System
    ^Fetus
    LP310004-9
    • System Core
      NULL
       
    • Super System
      Fetus
      LP6982-5
  • Scale
    Nar
    LP7749-7
  • Method
    Based on maternal age
    LP185800-2

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.50
Last Updated
Version 2.73 (MIN)
Order vs. Observation
Both

Member of these Panels

LOINCLong Common Name
96978-2Noninvasive prenatal fetal aneuploidy and 22q11.2 deletion panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA
75547-0Noninvasive prenatal fetal aneuploidy and microdeletion panel based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific circulating cell free (ccf) DNA
96977-4Noninvasive prenatal fetal aneuploidy panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Monozomie X předtestové riziko:Pravděpodobnost:Časový bod:^Plod:Narativní:Na základě věku matky
el-GRGreek (Greece)Προηγούμενος κίνδυνος μονοσωμίας Χ:Πιθανότητα:Pt:^Έμβρυο:Nar:Με βάση την ηλικία της μητέρας
Synonyms: - MOLPATH Nar Pt Έμβρυο Με βάση την ηλικία της μητέρας Πιθανότητα Προηγούμενος κίνδυνος μονοσωμίας Χ
es-ESSpanish (Spain)Riesgo previo de monosomía X:Probabilidad:Punto temporal:^Feto:Narrativo:Basado en edad materna
es-MXSpanish (Mexico)Riesgo previo de la monosomía X:Probabilidad:Punto temporal:^ Feto:Narrativo:Según la edad materna
fr-FRFrench (France)Risque prédominant monosomie X:Probabilité:Ponctuel:^foetus:Résultat textuel:Basé sur l'âge de la mère
it-ITItalian (Italy)Monosomia X, rischio preesistente:Probabilità:Pt:^feto:Nar:basato sull'età materna
Synonyms: Patologia molecolare Punto nel tempo (episodio) Rischio preesistente di monosomia X
zh-CNChinese (China)单体型 X 先验风险:似然性:时间点:^胎儿:叙述型:基于母亲年龄的方法
Synonyms: 分子病理学;分子病理学试验 单体型 X 先验风险（事前风险、事先风险）;X 单染色体症先验风险（危险性、风险性、危险）;特纳综合征先验风险;Turner 综合征先验风险;杜纳综合征先验风险;透纳氏症先验风险;透纳氏症候群先验风险;乌尔里希-特纳综合征先验风险;Ullrich-Turner 综合征先验风险;性腺发育不全先验风险;生殖腺发育不全先验风险;性腺发育障碍先验风险;性腺发育不良先验风险;性腺生殖力不全先验风险;性腺发育障碍症先验风险;Turner syndrome prior risk;Ullrich-Turner syndr 叙述;叙述性文字;报告;报告型;文字叙述;文本叙述型;文本描述;文本描述型 可能性;似然;可能 基于母亲（孕妇、产妇、孕产妇、妈妈）年龄的方法 时刻;随机;随意;瞬间 胎;超系统 - 胎儿

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=75568-6