LOINC Code 57037-4: Chr 13+18+21+X+Y aneuploidy Molgen Nom (Amn fld)

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 Chromosome 13+18+21+X+Y aneuploidy. It is commonly used with the system or sample type Amnio fld.

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: Both
• Method: Molgen

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• Chromosome 13+18+21+X+Y aneuploidy in Amniotic fluid by Molecular genetics method Nominal
• Chromosome 13+18+21+X+Y aneuploidy
• AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; Chr 13+18+21+X+Y aneup; Chromosom; Chromosomes; Finding; Findings; Molecular genetics; Molecular pathology; MOLPATH; Nominal; PCR; Point in time; Random

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