Germline disorder chromosome analysis in Amniotic fluid or Chorionic villus sample by Mate pair sequencing 94587-3
LOINC Code
LOINC code | 94587-3 | ||
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name | Germline disorder chromosome analysis in Amniotic fluid or Chorionic villus sample by Mate pair sequencing | ||
description | This term is used for the order & overall report for chromosome analysis by sequencing methods, such as mate pair sequencing, for the detection of germline (congenital) chromosome abnormalities in amniotic fluid or chorionic villus sampling (CVS) specimens. Results may include the overall findings, the result in ISCN format, testing methods, interpretation, recommendations, and references. Testing is performed when previous cytogenetic studies are unsuccessful or detect a chromosome abnormality of unknown significance. Results provide diagnostic, prognostic, and therapeutic information for patient care. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Germline disorder chromosome analysis | ||
property | Find = Finding | ||
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 | Amnio fld/CVS Amnio fld = Amniotic fluid | ||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
method | Mate pair sequencing | ||
Additional Names | |||
short name | Germline chromo analy Amn/CVS MPSeq | ||
Basic Attributes | |||
class | MOLPATH | ||
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 | 2.68 | ||
last change type | ADD - added | ||
Related Names | |||
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