LOINC Code 91680-9: F8 gene intron 22 inversion 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 F8 gene intron 22 inversion 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

• F8 gene intron 22 inversion targeted mutation analysis in Amniotic fluid or Chorionic villus sample by Molecular genetics method
• F8 gene intron 22 inversion targeted mutation analysis
• AF; AHF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Classic hemophilia; Coagulation Factor VIII gene; coagulation factor VIII, procoagulant component; Document; DXS1253E; F8 intron 22 Inv; F8B; F8C; Factor 8; Finding; Findings; FVIII; FVIII gene; Haemophilia; HEMA; Hemophilia A; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.INV; Mut; Mut Anl; Mutations; PCR; Point in time; Procoagulant component; 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