LOINC Code 34513-2: NPHS1 gene targeted mutation analysis Molgen Doc (Body fld)

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 NPHS1 gene targeted mutation analysis. It is commonly used with the system or sample type Body fld.

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

• NPHS1 gene targeted mutation analysis in Body fluid by Molecular genetics method
• NPHS1 gene targeted mutation analysis
• B/F; BF; bod; Bodies; Body fluid; Body fluid, unsp; CNF; Document; Finding; Findings; Fl; Fld; FLU; Fluid; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; nephrin; nephrosis 1, congenital, Finnish type; nephrosis 1, congenital, Finnish type (nephrin); NPHN; PCR; Point in time; Random

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