77015-6
LOINC Code
| LOINC code | 77015-6 | ||
|---|---|---|---|
| name | |||
| description | This term was created for, but is not limited in use to, Sequenom Laboratories' VisibiliT Trisomy 18 test, which analyzes circulating cell-free DNA extracted from maternal plasma using whole genome sequencing to determine the risk for fetal chromosome 18 aneuploidy. VisibiliT is indicated for use in pregnant women with average risk for fetal chromosomal aneuploidy. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Fetal trisomy 18 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 | Plas.cfDNA | ||
| scale | Ord = Ordinal: Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive. | ||
| method | Sequencing | ||
Additional Names | |||
| short name | Edward syndrome; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Impression; Impression/interpretation of study; Impressions; Inherited; Interp; Interpretation; Molecular pathology; MOLPATH; MOLPATH.TRISOMY; Next generation sequencing; NGS | ||
Basic Attributes | |||
| class | MOLPATH.TRISOMY | ||
| type | 1 Laboratory | ||
| order vs. observation | Fet Ts 18 risk | ||
Member of these Panels | |||
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History/Usage | |||
| first released | |||
| last updated | 2.73 | ||
| last change type | MIN - change to field other than name | ||
Related Names | |||
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