RHCE gene allele Cc [Genotype] in Amniotic fluid by Molecular genetics method Nominal 46731-6
LOINC Code
| LOINC code | 46731-6 | ||
|---|---|---|---|
| name | RHCE gene allele Cc [Genotype] in Amniotic fluid by Molecular genetics method Nominal | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | RHCE gene allele Cc | ||
| property | Geno = Genotype | ||
| 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 | Amnio fld = Amniotic fluid | ||
| 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 | RHCE allele Cc Geno Amn | ||
Basic Attributes | |||
| class | MOLPATH.MUT | ||
| 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. | |||
Member of these Panels | |||
History/Usage | |||
| first released | |||
| last updated | 2.68 | ||
| last change type | NAM - change to Analyte/Component | ||
| change reason | Release 2.68: COMPONENT: Updated to align with the LOINC term naming model for concepts used to report allelic genotypes (e.g. C/c, C/C, c/c.), which was the original intent for this term.; Previous Releases: Based on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section. | ||
Related Names | |||
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