99971-4Hemophagocytic lymphohistiocytosis multigene analysis in Blood or Tissue by Molecular genetics methodActive
Term 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.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Hemophagocytic lymphohistiocytosis multigene analysis
- Property
- Find
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Doc
- Method
- Molgen
Additional Names
- Short Name
- HLH multigene analysis Bld/T
- Display Name
- Hemophagocytic lymphohistiocytosis multigene analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha
- Hemophagocytic lymphohistiocytosis multigene analysis, Blood or tissue specimen
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.72
- Last Updated
- Version 2.72
- Order vs. Observation
- Both
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https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=99971-4
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