AutoICD API

50722-8

Laboratory

VKORC1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

Definition

The presence of the heterozygous missense mutation -1639 G>A in the VKORC1 gene can result in warfarin resistance. VKORC1 DNA analysis is performed by PCR followed by restriction enzyme digestion to detect -1639 G>A.

LOINC 6-Axis Classification

Component

VKORC1 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.PHARMG

Order/Observation

Both

Short Name

VKORC1 gene Mut Anl Bld/T

Display Name

VKORC1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodEDTP308GeneticsHeredityHeritableIdentity or presenceIMAGE3455200InheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.PHARMGMST134MST576MutMut AnlMutationsNominalPCRPoint in timeRandomTissueTissue, unspecifiedvitamin K epoxide reductase complex, subunit 1VKCFD2VKORWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 50722-8?

LOINC code 50722-8 identifies "VKORC1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". The presence of the heterozygous missense mutation -1639 G>A in the VKORC1 gene can result in warfarin resistance. VKORC1 DNA analysis is performed by PCR followed by restriction enzyme digestion to detect -1639 G>A.

What does 50722-8 measure?

This code measures VKORC1 gene targeted mutation analysis in Bld/Tiss. It belongs to the MOLPATH.PHARMG 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.