LOINC Code 41765-9: SCN1A 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 SCN1A 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

• SCN1A gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
• SCN1A gene targeted mutation analysis
• Blood; Document; EIEE6; FEB3; FEB3A; FHM3; Finding; Findings; GEFSP2; Genetics; HBSCI; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NAC1; Nav1.1; PCR; Point in time; Random; SCN1; SMEI; Sodium channel protein, brain I alpha subunit gene; sodium channel, voltage gated, type I alpha subunit; Sodium channel, voltage-gated, type I, alpha polypeptide gene; 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