LOINC Code 67816-9: Trisomy 18 + Trisomy 13 risk Qn (fetus)
67816-9 is a LOINC code used to identify Trisomy 18 + Trisomy 13 risk Qn (fetus) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Trisomy 18+Trisomy 13 risk. It is commonly used with the system or sample type ^Fetus.
What is this code?
LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Trisomy 18+Trisomy 13 risk. It is commonly used with the system or sample type ^Fetus.
When is it used?
- Used in lab systems, EHRs, and clinical data exchange.
- May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
- Status: ACTIVE
- Order vs observation: Observation
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- Trisomy 18 + Trisomy 13 risk [Likelihood] in Fetus
- Trisomy 18+Trisomy 13 risk
- Chemistry; Edward syndrome; Fetal; Gyn; Gynecology; OB; ObGyn; Obstetrics; Point in time; QNT; Quan; Quant; Quantitative; Random; Risk; Trisomy 18+13 risk; Ts
Where you may see this code
You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.
Common synonyms
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.