100754-1

LOINC Code


LOINC code100754-1
name
descriptionThis 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.
statusACTIVE

Fully-Specified Name

componentPlatelet disorders multigene analysis
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodSequencing

Additional Names

short nameBlood; Document; Finding; Findings; Gene; Gene panel; high-throughput sequencing; HTS; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; Next generation sequencing; NGS; Pl; Platelets; Platelt; Plt; Plt disorder gene anal; Point in

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationPlt disorder ge

History/Usage

first released
last updated2.73
last change typeADD  - added

Related Names

N

Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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