101538-7
LaboratorySMA residual risk [Interpretation] in Blood by Molecular genetics method Narrative
Definition
This test is based on sequencing and targeted analysis of specific variants . The testing depends largely upon the individual's ethnic background. A negative result may indicate a reduced carrier risk for some or all diseases being tested, this risk cannot be eliminated.
LOINC 6-Axis Classification
Component
SMA residual risk
Property
Imp
Time Aspect
Pt
System
Bld
Scale Type
Nar
Method Type
Molgen
Details
Class
MOLPATH.MUT
Order/Observation
Both
Short Name
SMA residual risk Bld-Imp
Display Name
SMA residual risk Molgen Nar (Bld) [Interp]
Related Names
Frequently Asked Questions
What is LOINC code 101538-7?
LOINC code 101538-7 identifies "SMA residual risk [Interpretation] in Blood by Molecular genetics method Narrative". This test is based on sequencing and targeted analysis of specific variants . The testing depends largely upon the individual's ethnic background. A negative result may indicate a reduced carrier risk for some or all diseases being tested, this risk cannot be eliminated.
What does 101538-7 measure?
This code measures SMA residual risk in Bld. 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.