Hereditary platelet function defect multigene analysis in Blood by Molecular genetics method 105333-9
LOINC Code
| LOINC code | 105333-9 | ||
|---|---|---|---|
| name | Hereditary platelet function defect multigene analysis in Blood by Molecular genetics method | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Hereditary platelet function defect 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 = Whole blood | ||
| 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 | Hered plat func def multi analy Bld | ||
Basic Attributes | |||
| class | MOLPATH | ||
| type | 1 Laboratory | ||
| order vs. observation | Order | ||
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 | 2.78 | ||
| last change type | ADD - added | ||
Related Names | |||
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