LOINC Code 75032-3: CEBPA gene full mutation analysis Sequencing Doc (BM)

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 CEBPA gene full mutation analysis. It is commonly used with the system or sample type Bone mar.

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

• CEBPA gene full mutation analysis in Bone marrow by Sequencing
• CEBPA gene full mutation analysis
• BM; BON; Bone marrow; C/EBP-alpha; CCAAT/enhancer binding protein (C/EBP), alpha; CEBP; Document; Familial AML; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; MAR; Marrow (bone); minimal angle of resolution; Minimum angle of resolution; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; Point in time; Random; sequencing of entire coding region

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