Type of Congenital cranial dysinnervation syndrome (CCDS) suspected   79736-5

LOINC Code


LOINC code79736-5
nameType of Congenital cranial dysinnervation syndrome (CCDS) suspected
descriptionThis term was developed in collaboration with the National Institute of Health's National Eye Institute (NEI) as part of an effort to standardize the data elements collected by the National Ophthalmic Disease Genotyping and Phenotyping Network (eyeGENE).
statusACTIVE

Fully-Specified Name

componentCongenital cranial dysinnervation syndrome (CCDS) suspected
propertyType  =  Type:  The Property Type is used for assays that identify the specific analyte in cases when the baseline presence of the analyte is known.
timePt  =  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^Patient
scaleNom  =  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

Additional Names

short nameType of CCDS susp

Basic Attributes

classEYE.HX.NEI
type2  Clinical
order vs. observationObservation

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 updated2.54
last change typeMIN  - change to field other than name

Related Names

CCDS susp
EYE
EYE.HX
EYE.HX.NEI
Nominal
Ophthalmology
Ophtho
Ophthy
Point in time
Random
Typ

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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