LOINC Code 105331-3: Hereditary bleeding disorders factor and von Willebrand multigene 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 Hereditary bleeding disorders factor and von Willebrand multigene 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

• Hereditary bleeding disorders factor and von Willebrand multigene analysis in Specimen by Molecular genetics method
• Hereditary bleeding disorders factor and von Willebrand multigene analysis
• Document; Fac; Fact; Finding; Findings; Gene; Gene panel; Hered bleed fact & Vw multi analy; Misc; Miscellaneous; Molecular genetics; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; Other; PCR; Point in time; Random; Spec; To be specified in another part of the message; Unspecified; Von will; Vonwillebrand; vWf

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