LOINC Code 75391-3: FGFR3 gene targeted mutation analysis Molgen Doc (Amnio fld/CVS)

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 FGFR3 gene targeted mutation analysis. It is commonly used with the system or sample type Amnio fld/CVS.

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

• FGFR3 gene targeted mutation analysis in Amniotic fluid or Chorionic villus sample by Molecular genetics method
• FGFR3 gene targeted mutation analysis
• ACH; Achondroplasia; AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; CD333; CEK2; Chorionic villi; Chorionic villus sample; Document; fibroblast growth factor receptor 3; Finding; Findings; Genetics; Gyn; Gynecology; Heredity; Heritable; HSFGFR3EX; Inherited; JTK4; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; OB; ObGyn; Obstetrics; PCR; Point in time; Random; Thanatophoric dwarfism; Thanatophoric dysplasia

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