LOINC Code 105333-9: Hereditary platelet function defect multigene analysis Molgen Doc (Bld)

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 platelet function defect multigene analysis. It is commonly used with the system or sample type Bld.

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 platelet function defect multigene analysis in Blood by Molecular genetics method
• Hereditary platelet function defect multigene analysis
• Blood; Closure time; Closure Tme; Document; FCN; Finding; Findings; Func; Funct; Gene; Gene panel; Hered plat func def multi analy; Molecular genetics; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; PCR; Pl; Platelets; Platelt; Plt; Point in time; Random; Thrombocyte; Thrombocytes; WB; Whole blood

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