AutoICD API

91681-7

Laboratory

F9 gene mutation analysis limited to known familial mutations in Amniotic fluid or Chorionic villus sample by Molecular genetics method

LOINC 6-Axis Classification

Component

F9 gene mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Amnio fld/CVS

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

F9 gene Fam Mut Anl Amn/CVS

Display Name

F9 gene familial mut analysis Molgen Doc (Amnio fld/CVS)

Related Names

AFAmnAmn flAmn/CVSAmnioAmniotic fluAmniotic fluidChorionic villiChorionic villus sampleChristmas factorCoagulation Factor 9 genecoagulation factor IXCoagulation Factor IX geneDocumentFam Mut AnlFindingFindingsFIXHEMBLMTEDLTDMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationMutationsMutsP19PCRPoint in timePTCRandomTHPH8

Frequently Asked Questions

What is LOINC code 91681-7?

LOINC code 91681-7 identifies "F9 gene mutation analysis limited to known familial mutations in Amniotic fluid or Chorionic villus sample by Molecular genetics method". It measures F9 gene mutation analysis limited to known familial mutations in Amnio fld/CVS.

What does 91681-7 measure?

This code measures F9 gene mutation analysis limited to known familial mutations in Amnio fld/CVS. 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.