Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel:-:Pt:Ser/Plas:-:

Preferred Label : Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel:-:Pt:Ser/Plas:-:;

LOINC status : ACTIVE;

LOINC display name : Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel;

LOINC long common name : Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel - Serum or Plasma;

LOINC short name : Mat scn for fetal abnormalities SerPl;

LOINC 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.;

Details

Origin ID

50580-0;

UMLS CUI

C1978522;

Has component
- Maternal screen for fetal abnormalities such as Open Neural Tube Defects, Trisomy 21 or Trisomy 18 panel [LOINC component]
- Trisomy 21 [LOINC component]
Has system
- Plasma [LOINC System]
- Serum [LOINC System]
- Serum or Plasma [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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