HBB gene full mutation analysis in Amniotic fluid or Chorionic villus sample by Sequencing   90925-9

LOINC Code


LOINC code90925-9
nameHBB gene full mutation analysis in Amniotic fluid or Chorionic villus sample by Sequencing
statusACTIVE

Fully-Specified Name

componentHBB gene full mutation analysis
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemAmnio fld/CVS
    Amnio fld  =  Amniotic fluid
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodSequencing

Additional Names

short nameHBB gene Full Mut Anl Amn/CVS Seq

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationBoth

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.65
last change typeADD  - added

Related Names

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

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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