Log In

Part Description

LP99499-3   Fetal trisomy 13 risk
Trisomy 13 risk refers to the fetus's risk of having trisomy 13. The risk can be estimated based on maternal age as well as prenatal genetic testing of fetal DNA. Trisomy 13, also called Patau syndrome, is caused by the presence of three copies of chromosome 13 in each cell rather than two. Patau syndrome is associated with severe cognitive delay, various forms of congenital heart disease, brain or spinal cord abnormalities, hypotonia, cleft lip and/or palate, and poorly developed eyes. Many liveborn infants with Patau syndrome die within the first weeks of life, and less than 10% survive longer than one year. The general population risk of Trisomy 13 is about 1 in 16,000 live births, but the risk increases with increasing maternal age. [MedlinePlus Condition: trisomy-13] Source: Regenstrief LOINC, GHR: Trisomy 13

LOINC Names Get Info

Fully-Specified Name
Fetal trisomy 13 risk:Likelihood:Pt:^Fetus:Qn:
Long Common Name
Trisomy 13 risk [Likelihood] in Fetus
Short Name
Ts 13 risk Fetus
Display Name
Trisomy 13 risk Qn (fetus)
Consumer Name Alpha Get Info
Fetal Trisomy 13 risk

Part Model Get Info

  • Component
    Fetal trisomy 13 risk
    LP99499-3
    • Analyte
      Fetal trisomy 13 risk
      LP99499-3
      • Component Numerator
        Fetal trisomy 13 risk
        LP99499-3
        • Component Numerator Core
          Fetal trisomy 13 risk
          LP99499-3
        • 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
    Qn
    LP7753-9
  • Method
    NULL
     

Basic Attributes

Class
CHEM
Type
Laboratory
First Released
Version 2.32
Last Updated
Version 2.73 (MIN)
Change Reason
Added "Fetal" to Component for consistency across terms that represent fetal risk and vary by System
Order vs. Observation
Observation
Common Test Rank Get Info
6288

Language Variants Get Info

TagLanguageTranslation
ar-JOArabic (Jordan)الكشف عن احتمالية خطر إصابة الجنين بالتثلث الصبغي 13
cs-CZCzech (Czechia)Trizomie 13 riziko u plodu:Pravděpodobnost:Časový bod:^Plod:Kvantitativní:
el-GRGreek (Greece)Κίνδυνος εμβρυϊκής τρισωμίας 13:Πιθανότητα:Pt:^Έμβρυο:Qn:
Synonyms: - CHEM Pt Qn Έμβρυο Κίνδυνος εμβρυϊκής τρισωμίας 13 Πιθανότητα
es-ESSpanish (Spain)Riesgo de trisomía 13:Probabilidad:Punto temporal:^Feto:Qn:
Synonyms: Cuantitativo
es-MXSpanish (Mexico)Riesgo de trisomía 13 fetal:Probabilidad:Punto temporal:^ Feto:Cuantitativo:
fr-FRFrench (France)Risque de trisomie 13 foetale:Probabilité:Ponctuel:^foetus:Numérique:
fr-CAFrench (Canada)Risque de trisomie 13 fœtal:Probabilité:Temps ponctuel:^Foetus:Quantitatif:
it-ITItalian (Italy)Trisomia 13, rischio:Probabilità:Pt:^feto:Qn:
Synonyms: Chimica Punto nel tempo (episodio) Rischio di trisomia 13
nl-NLDutch (Netherlands)risico op foetus met trisomie 13:waarschijnlijkheid:moment:^foetus:kwantitatief:
Synonyms: risico op foetale trisomie 13
pl-PLPolish (Poland)Ryzyko trisomii 13 u płodu:prawdopodobieństwo:punkt w czasie:^płód:ilościowy:
Synonyms: Ryzyko trisomii chromosomu 13 u płodu
pt-BRPortuguese (Brazil)Trisomia 13 risco:Achado:Pt:^Feto:Qn:
tr-TRTurkish (Turkey)Trizomi 13 riski:Olabilirlik:Zmlı:^Fetus:Kant:
zh-CNChinese (China)胎儿三体型 13 风险:似然性:时间点:^胎儿:定量型:
Synonyms: 三体型 三体细胞 三染色体性 三染色体细胞 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 可用数量表示的;定量性;数值型;数量型;连续数值型标尺 可能性;似然;可能 时刻;随机;随意;瞬间 胎;超系统 - 胎儿 胎儿 13 三体型综合征风险（危险性、风险性、危险）;13 三体型风险;13 三体性综合征风险;13 三体性风险;13 三体综合征风险;13 号染色体三体型风险;13 号染色体三体性风险;T13 风险;Ts 13 风险;三体性 13 风险;染色体 13 三体型风险;染色体 13 三体性风险;13-三体综合征风险;13 号染色体三体型综合征风险;Patau 综合征风险;帕套综合征风险

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=58769-1