LOINC Code 103950-2: NOTCH3 gene full 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 NOTCH3 gene full 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: Both
• Method: Molgen

What it does not mean

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

Key facts

• NOTCH3 gene full mutation analysis in Specimen by Molecular genetics method
• NOTCH3 gene full mutation analysis
• CADASIL; CASIL; cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; Document; Finding; Findings; full gene sequencing; Full Mut Anl; IMF2; Misc; Miscellaneous; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; notch 3; Notch homolog 3; NOTCH3 full mut anlyss; Other; PCR; Point in time; Random; sequencing of entire coding region; Spec; To be specified in another part of the message; Unspecified

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