LOINC Code 81876-5: SPG11 gene del+dup and 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 SPG11 gene deletion+duplication & 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

• SPG11 gene deletion+duplication and mutation analysis in Blood or Tissue by Molecular genetics method
• SPG11 gene deletion+duplication & mutation analysis
• ALS5; Amplification; Blood; CMT2X; Del; Del+Dup; Del+Dup + Mut Anl; Deletions; Document; Dp; Finding; Findings; Genetics; Heredity; Heritable; Inherited; KIAA1840; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Mut; Mutations; PCR; Point in time; Random; spastic paraplegia 11 (autosomal recessive); 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