AutoICD API

32632-2

Laboratory

HEXA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

HEXA gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

HEXA gene Mut Anl Bld/T

Display Name

HEXA gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

beta-N-acetylhexosaminidase geneBloodGeneticsGM2-gangliosidosisHeredityHeritablehexosaminidase A (alpha polypeptide)hexosaminidase A (alpha polypeptide) geneIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsN-acetyl-beta-glucosaminidase geneNominalPCRPoint in timeRandomTay-Sachs diseaseTissueTissue, unspecifiedTSDUniversalLabOrdersWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 32632-2?

LOINC code 32632-2 identifies "HEXA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures HEXA gene targeted mutation analysis in Bld/Tiss.

What does 32632-2 measure?

This code measures HEXA gene targeted mutation analysis in Bld/Tiss. It belongs to the MOLPATH.MUT class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.