AutoICD API

41750-1

Laboratory

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

LOINC 6-Axis Classification

Component

COCH 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

COCH gene Mut Anl Bld/T

Display Name

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

Related Names

BloodCoagulation factor C homolog, cochlin (Limulus polyphemus)COCH5B2COCH-5B2cochlinCochlin precursorDeafness, autosomal dominant 9DFNA31DFNA9GeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41750-1?

LOINC code 41750-1 identifies "COCH gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures COCH gene targeted mutation analysis in Bld/Tiss.

What does 41750-1 measure?

This code measures COCH 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.