Hemophagocytic lymphohistiocytosis multigene analysis in Blood or Tissue by Molecular genetics method 99971-4
LOINC Code
LOINC code | 99971-4 | ||
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name | Hemophagocytic lymphohistiocytosis multigene analysis in Blood or Tissue by Molecular genetics method | ||
description | Multigene analysis for hemophagocytic lymphohistiocytosis (HLH), a syndrome characterized by hyperactivation of the immune system, excessive cytokine secretion and severe systemic inflammation. HLH is classified as familial (FHL) when associated with mutations in specific genes, such as PRF1, UNC13D, STX11, and STXBP2 genes.[PMID: 33746956] Testing is performed for diagnostic, prognostic, and therapeutic assessment in patients with HLH. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Hemophagocytic lymphohistiocytosis 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 | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
short name | HLH multigene analysis Bld/T | ||
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 | 2.72 | ||
last change type | ADD - added | ||
Related Names | |||
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