HEXA gene full mutation analysis in Blood or Tissue by Sequencing 76033-0
LOINC Code
LOINC code | 76033-0 | ||
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name | HEXA gene full mutation analysis in Blood or Tissue by Sequencing | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | HEXA 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 | HEXA gene Full Mut Anl Bld/T Seq | ||
Basic Attributes | |||
class | MOLPATH.MUT | ||
type | 1 Laboratory | ||
order vs. observation | Both | ||
Ask At Order Entry | |||
Ask at Order Entry (AOE) observations for a clinical observation or laboratory test. A LOINC term may represent a single AOE observation or a panel containing several AOE observations.
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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 | |||
test rank | 19983 of 2000 most commonly performed tests by labs in USA | ||
first released | |||
last updated | 2.73 | ||
last change type | MIN - change to field other than name | ||
change reason | Updated Scale from "Nar" to "Doc" since results can be reported in narrative or structured format, which is represent as "Doc" in LOINC. Based on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats. | ||
Related Names | |||
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