LOINC Code 101388-7: GP1BB full 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 GP1BB 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: Molgen

What it does not mean

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

Key facts

• GP1BB full mutation analysis in Blood or Tissue by Molecular genetics method
• GP1BB gene full mutation analysis
• Bernard Soulier syndrome; beta polypeptide; Blood; CD42c; Document; Finding; Findings; full gene sequencing; Full Mut Anl; GP1BB full mutation analysis; GPIbbeta; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; PCR; platelet glycoprotein Ib beta chain; Point in time; Random; sequencing of entire coding region; 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