LOINC Code 34514-0: SLC22A18 gene targeted mutation analysis Molgen Doc (Bld/Tiss)

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 SLC22A18 gene targeted mutation analysis. It is commonly used with the system or sample type Bld/Tiss.

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

• SLC22A18 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
• SLC22A18 gene targeted mutation analysis
• Beckwith-Wiedemann syndrome chromosome region 1, candidate a; Blood; BWR1A; BWSCR1A; Document; Finding; Findings; Genetics; Heredity; Heritable; HET; imprinted polyspecific membrane transporter 1; IMPT1; Inherited; ITM; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; ORCTL2; organic cation transporter-like 2; p45-BWR1A; PCR; Point in time; Random; SLC22A1L; Solute carrier family 22 (organic cation transporter), member 18; solute carrier family 22 (organic cation transporter), member 1-like; solute carrier family 22, member 18; Tissue; Tissue, unspecified; TSSC5; WB; Whole blood; Whole blood or Tissue

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