AutoICD API

32653-8

Laboratory

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

Definition

Familial dysautonomia is a hereditary disorder affecting the autonomic nervous system.

LOINC 6-Axis Classification

Component

DYS 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

DYS gene Mut Anl Bld/T

Display Name

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

Related Names

BloodDYSDysautonomiaELP1Familial dysatonomiaFDGeneticsHeredityHeritableIdentity or presenceIKAPIKBKAPIKI3Inheritedinhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated proteinMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeRandomRiley-Day syndromeTissueTissue, unspecifiedTOT1WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 32653-8?

LOINC code 32653-8 identifies "DYS gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". Familial dysautonomia is a hereditary disorder affecting the autonomic nervous system.

What does 32653-8 measure?

This code measures DYS 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.