100754-1LOINC 2.82
Platelet disorders multigene analysis in Blood or Tissue by Sequencing
Plt disorder gene anal Bld/T Seq
Definition
- 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.
Component
- Platelet disorders multigene analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- Blood; 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 time; Random; Thrombocyte; Thrombocytes; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- 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 time
- Random
- Thrombocyte
- Thrombocytes
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue