AutoICD API

41116-5

Laboratory

ATP7A gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

ATP7A 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

ATP7A gene Mut Anl Bld/T

Display Name

ATP7A gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

ATPase, Cu++ transporting, alpha polypeptideBloodDSMAXGeneticsHeredityHeritableIdentity or presenceInheritedMC1Menkes syndromeMKMNKMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalOccipital horn syndromeOHSPCRPoint in timeRandomSMAX3TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41116-5?

LOINC code 41116-5 identifies "ATP7A gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures ATP7A gene targeted mutation analysis in Bld/Tiss.

What does 41116-5 measure?

This code measures ATP7A 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.