82535-6
LaboratoryKRAS gene full mutation analysis in Blood or Tissue by Sequencing
Definition
Full sequencing analysis of all coding exons and intron/exon boundaries of the KRAS gene is performed to establish a diagnosis of KRAS-associated Noonan syndrome, cardiofaciocutaneous syndrome, Costello syndrome, and clinically related disorders.[OMIM: 190070][GHR gene: KRAS]
LOINC 6-Axis Classification
Component
KRAS gene full mutation analysis
Property
Find
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Doc
Method Type
Sequencing
Details
Class
MOLPATH.MUT
Order/Observation
Both
Short Name
KRAS gene Full Mut Anl Bld/T Seq
Display Name
KRAS gene full mutation analysis Sequencing Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 82535-6?
LOINC code 82535-6 identifies "KRAS gene full mutation analysis in Blood or Tissue by Sequencing". Full sequencing analysis of all coding exons and intron/exon boundaries of the KRAS gene is performed to establish a diagnosis of KRAS-associated Noonan syndrome, cardiofaciocutaneous syndrome, Costello syndrome, and clinically related disorders.[OMIM: 190070][GHR gene: KRAS]
What does 82535-6 measure?
This code measures KRAS gene full 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.