LOINC Code 90925-9: HBB gene full mutation analysis Sequencing 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 HBB gene full 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: Sequencing

What it does not mean

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

Key facts

• HBB gene full mutation analysis in Amniotic fluid or Chorionic villus sample by Sequencing
• HBB gene full mutation analysis
• AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Beta globulin gene; Beta thalessemia; beta-globin; CD113t-C; Chorionic villi; Chorionic villus sample; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Gyn; Gynecology; Hemoglobin beta chain; Hemoglobin S gene; hemoglobin, beta; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; OB; ObGyn; Obstetrics; Point in time; Random; sequencing of entire coding region; Sickle cell anemia

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