LOINC Code 38919-7: LITAF gene targeted mutation analysis Molgen Nom (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 LITAF 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

• LITAF gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
• LITAF gene targeted mutation analysis
• Blood; Charcot-Marie Tooth disease, type 1C; CMT1C; FLJ38636; Genetics; Heredity; Heritable; Identity or presence; Inherited; lipopolysaccharide-induced TNF factor; Lipopolysaccharide-induced tumor necrosis factor-alpha factor; LPS-induced TNF-alpha factor; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; PIG7; Point in time; Random; SIMPLE; Small integral membrane protein of lysosome/late endosome; Tissue; Tissue, unspecified; TP53I7; Tumor protein p53 inducible protein 7; 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