AutoICD API

41056-3

Laboratory

SLC22A18 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

SLC22A18 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

SLC22A18 gene Mut Anl Bld/T

Display Name

SLC22A18 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

Beckwith-Wiedemann syndrome chromosome region 1, candidate aBloodBWR1ABWSCR1AGeneticsHeredityHeritableHETIdentity or presenceimprinted polyspecific membrane transporter 1IMPT1InheritedITMMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalORCTL2organic cation transporter-like 2p45-BWR1APCRPoint in timeRandomSLC22A1LSolute carrier family 22 (organic cation transporter), member 18solute carrier family 22 (organic cation transporter), member 1-likesolute carrier family 22, member 18TissueTissue, unspecifiedTSSC5WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41056-3?

LOINC code 41056-3 identifies "SLC22A18 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures SLC22A18 gene targeted mutation analysis in Bld/Tiss.

What does 41056-3 measure?

This code measures SLC22A18 gene targeted mutation analysis in Bld/Tiss. It belongs to the MOLPATH.MUT 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.