Genetic disease assessed [ID] 51967-8
LOINC Code
LOINC code | 51967-8 | ||
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name | Genetic disease assessed [ID] | ||
description | Coded identifier of the disorder being assessed but with exception to allow the recording of something not included in the controlled vocabulary that is being used. Various coding systems may be used, including ICD-9-CM, ICD-10-CM, SCT and NCBI MedGen. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Genetic disease assessed | ||
property | ID = Identifier | ||
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 | Gene dis assessed | ||
Basic Attributes | |||
class | HL7.GENETICS | ||
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. | |||
Member of these Panels | |||
History/Usage | |||
first released | |||
last updated | 2.58 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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