Kallmann syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal 21701-8
LOINC Code
| LOINC code | 21701-8 | ||
|---|---|---|---|
| name | Kallmann syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Kallmann syndrome gene mutations tested for | ||
| property | Prid = Presence or identity: Prid stands for “Presence or identity”, is used for assays that detect whether or not an analyte of a particular kind is present, and if it is, to identify the specific analyte. | ||
| 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 | Nom = Nominal: Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody. | ||
| 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 | KMS gene Mut Tested Bld/T | ||
Basic Attributes | |||
| class | MOLPATH.MUT | ||
| type | 1 Laboratory | ||
| order vs. observation | Observation | ||
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 | 2.67 | ||
| last change type | NAM - change to Analyte/Component | ||
| change reason | Release 2.67: COMPONENT: Corrected typo | ||
Related Names | |||
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