Platelet disorders multigene analysis in Blood or Tissue by Sequencing 100754-1
LOINC Code
LOINC code | 100754-1 | ||
---|---|---|---|
name | Platelet disorders multigene analysis in Blood or Tissue by Sequencing | ||
description | This LOINC code can be used for analysis of genes including but not limited to the following: ANO6, AP3B1, BLOC1S3, BLOC1S6,DTNBP1, FGA, FGB, FGG, GP1BA, GP1BB, GP6, GP9, HPS1, HPS3, HPS4, HPS5, HPS6, ITGA2B, ITGB3, LYST, MYH9, P2RY12, PLA2G7, PLAU, RASGRP2, TBXA2R, TBXAS1, VIPAS39, VPS33B, VWF, WAS. Disease diagnosed can include Glanzmann's Thrombasthenia, Bernard-Soulier Syndrome, and others. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Platelet disorders multigene 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 | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
method | Sequencing | ||
Additional Names | |||
short name | Plt disorder gene anal Bld/T Seq | ||
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 | 2.73 | ||
last change type | ADD - added | ||
Related Names | |||
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