AutoICD API

57029-1

Laboratory

Fetal chromosome 13+18+21+X+Y aneuploidy in Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

Fetal chromosome 13+18+21+X+Y aneuploidy

Property

Find

Time Aspect

Pt

System

Tiss^Fetus

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Both

Short Name

Chr 13+18+21+X+Y aneup Tiss Fetus

Display Name

Chr 13+18+21+X+Y aneuploidy Molgen Nom (Tiss fetus)

Related Names

Chr 13+18+21+X+Y aneupChromosomChromosomesFetalFindingFindingsGynGynecologyMolecular geneticsMolecular pathologyMOLPATHNominalOBObGynObstetricsPCRPoint in timeRandomTissueTissue, unspecified

Frequently Asked Questions

What is LOINC code 57029-1?

LOINC code 57029-1 identifies "Fetal chromosome 13+18+21+X+Y aneuploidy in Tissue by Molecular genetics method Nominal". It measures Fetal chromosome 13+18+21+X+Y aneuploidy in Tiss^Fetus.

What does 57029-1 measure?

This code measures Fetal chromosome 13+18+21+X+Y aneuploidy in Tiss^Fetus. It belongs to the MOLPATH 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.