AutoICD API

32639-7

Laboratory

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

LOINC 6-Axis Classification

Component

FANCC 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

FANCC gene Mut Anl Bld/T

Display Name

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

Related Names

BloodFA3FACFACCFalconi's Anemia Complementation group CFanconi anemia, complementation group CGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 32639-7?

LOINC code 32639-7 identifies "FANCC gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures FANCC gene targeted mutation analysis in Bld/Tiss.

What does 32639-7 measure?

This code measures FANCC 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.