LOINC Code 45331-6: NF1 gene targeted mutation analysis Molgen Nom (Amn 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 NF1 gene targeted mutation analysis. It is commonly used with the system or sample type Amnio 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

• NF1 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal
• NF1 gene targeted mutation analysis
• AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; Genetics; Gyn; Gynecology; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Neurofibromatosis; Neurofibromin 1; NFNS; Nominal; OB; ObGyn; Obstetrics; PCR; Point in time; Random; von Recklinghausen disease; VRNF; Watson disease; WSS

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