LOINC Code 41115-7: NOD2 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 NOD2 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

• NOD2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
• NOD2 gene targeted mutation analysis
• ACUG; Arthrocutaneouveal granulomatosis (Blau syndrome); BLAU; Blau syndrome, granulomatous synovitis with uveitis and cranial neuropathies; Blood; CARD15; Caspase recruitment domain family, member 15; CD; CLR16.3; Crohn disease; Genetics; Heredity; Heritable; IBD1; Identity or presence; Inflammatory bowel disease 1; Inherited; LRR-containing protein gene; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NLRC2; NOD2; NOD2B; Nominal; nucleotide-binding oligomerization domain containing 2; Nucleotide-binding oligomerization domain protein 2 gene; PCR; Point in time; PSORAS1; 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