SMA residual risk [Interpretation] in Blood by Molecular genetics method Narrative 101538-7
LOINC Code
| LOINC code | 101538-7 | ||
|---|---|---|---|
| name | SMA residual risk [Interpretation] in Blood by Molecular genetics method Narrative | ||
| description | 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. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | SMA residual risk | ||
| property | Imp = Impression/interpretation of study | ||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
| system | Bld = Whole blood | ||
| scale | Nar = Narrative: Text narrative, such as the description of a microscopic part of a surgical papule test. | ||
| method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
| short name | SMA residual risk Bld-Imp | ||
Basic Attributes | |||
| class | MOLPATH.MUT | ||
| type | 1 Laboratory | ||
| order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
| first released | |||
| last updated | 2.75 | ||
| last change type | MIN - change to field other than name | ||
Related Names | |||
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