Preferred Label : Platelet disorders multigene analysis:Find:Pt:Bld/Tiss:Doc:Sequencing;
LOINC status : ACTIVE;
LOINC display name : Platelet disorders multigene analysis Sequencing Doc (Bld/Tiss);
LOINC long common name : Platelet disorders multigene analysis in Blood or Tissue by Sequencing;
LOINC short name : Plt disorder gene anal Bld/T Seq;
LOINC 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.;
Origin ID : 100754-1;
UMLS CUI : C5689460;
Has component
- Has method
- Has property
- Has scale
- Has system
- Has time aspect
- Semantic type(s)
