LOINC Code 53875-1: LMX1B 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 LMX1B 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

• LMX1B gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
• LMX1B gene targeted mutation analysis
• Blood; Document; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LIM homeo box transcription factor 1, beta; LIM homeobox transcription factor 1, beta; LIM/homeobox protein 1.2; LIM/homeobox protein LMX1B; LMX1.2; LMX-1.2; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NPS1; PCR; Point in time; Random; Tissue; Tissue, unspecified; 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