67816-9
LaboratoryTrisomy 18 + Trisomy 13 risk [Likelihood] in Fetus
LOINC 6-Axis Classification
Component
Trisomy 18+Trisomy 13 risk
Property
Likelihood
Time Aspect
Pt
System
^Fetus
Scale Type
Qn
Method Type
N/A
Details
Class
CHEM
Order/Observation
Observation
Short Name
Trisomy 18+13 risk Fetus
Display Name
Trisomy 18 + Trisomy 13 risk Qn (fetus)
Related Names
ChemistryEdward syndromeFetalGynGynecologyOBObGynObstetricsPoint in timeQNTQuanQuantQuantitativeRandomRiskTrisomy 18+13 riskTs
Frequently Asked Questions
What is LOINC code 67816-9?
LOINC code 67816-9 identifies "Trisomy 18 + Trisomy 13 risk [Likelihood] in Fetus". It measures Trisomy 18+Trisomy 13 risk in ^Fetus.
What does 67816-9 measure?
This code measures Trisomy 18+Trisomy 13 risk in ^Fetus. It belongs to the CHEM class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.