AutoICD API

41109-0

Laboratory

FGD1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

FGD1 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

FGD1 gene Mut Anl Bld/T

Display Name

FGD1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

AASBloodFaciogenital dysplasia (Aarskog-Scott syndrome)FGDYFYVE, RhoGEF and PH domain containing 1FYVE, RhoGEF and PH domain containing 1 (faciogenital dysplasia)GeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMRXS16MutMut AnlMutationsNominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or TissueZFYVE3

Frequently Asked Questions

What is LOINC code 41109-0?

LOINC code 41109-0 identifies "FGD1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures FGD1 gene targeted mutation analysis in Bld/Tiss.

What does 41109-0 measure?

This code measures FGD1 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.