THBD gene full mutation analysis in Blood or Tissue by Sequencing 92995-0
LOINC Code
LOINC code | 92995-0 | ||
---|---|---|---|
name | THBD gene full mutation analysis in Blood or Tissue by Sequencing | ||
description | This test detects alterations in the THBD gene, which have been associated with one of several clinical phenotypes and hereditary disorders, namely an increased risk for thrombosis, atypical hemolytic uremic syndrome (aHUS), and hereditary excessive bleeding following physical trauma or surgery. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | THBD gene full mutation 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 | Sequencing | ||
Additional Names | |||
short name | THBD gene Full Mut Anl Bld/T Seq | ||
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 | 2.66 | ||
last change type | ADD - added | ||
Related Names | |||
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