Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics method 99967-2
LOINC Code
| LOINC code | 99967-2 | ||
|---|---|---|---|
| name | Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics method | ||
| description | Multigene testing for atypical hemolytic uremic syndrome (aHUS), a condition that can begin in the neonatal period to adulthood and consists of hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the kidney and other organs. Genes associated with genetic aHUS include C3, C5, CD46, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, DGKE, PLG, THBD, and MMACHC. Testing is performed for diagnostic, prognostic, and therapeutic assessment in patients with aHUS.[NCBI Books: NBK1367] | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Atypical hemolytic uremic syndrome 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 | aHUS 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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