LOINC Code 105337-0: VWF and GP1BA gene mutation analysis Molgen Doc (Specimen)

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 VWF and GP1BA gene mutation analysis. It is commonly used with the system or sample type XXX.

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: Order
• Method: Molgen

What it does not mean

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

Key facts

• VWF and GP1BA gene mutation analysis in Specimen by Molecular genetics method
• VWF and GP1BA gene mutation analysis
• alpha polypeptide; CD42b; Document; Finding; Findings; GP1B; Misc; Miscellaneous; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; Other; PCR; platelet glycoprotein Ib alpha chain; Point in time; Random; Spec; To be specified in another part of the message; Unspecified; VWF and GP1BA mut analy

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