LOINC Code 94215-1: PRSS1 gene full mutation analysis Sequencing 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 PRSS1 gene full 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: Sequencing

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• PRSS1 gene full mutation analysis in Blood or Tissue by Sequencing
• PRSS1 gene full mutation analysis
• Full sequence analysis to test for the presence of a mutation in all coding regions and intron/exon boundaries of the PRSS1 gene. Testing is used to confirm the diagnosis of hereditary pancreatitis (HP) in patients with chronic pancreatitis and allow for predictive and diagnostic testing in affected family members.
• Blood; Cationic trypsinogen; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Hereditary pancreatitis; Heredity; Heritable; high-throughput sequencing; HPC; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; PCTT; Point in time; protease, serine, 1 (trypsin 1); Random; sequencing of entire coding region; Tissue; Tissue, unspecified; TRP1; TRY1; TRY4; TRYP1; Trypsin 1 precursor; Trypsinogen 1; 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