Kallmann syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal   21701-8

LOINC Code


LOINC code21701-8
nameKallmann syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal
statusACTIVE

Fully-Specified Name

componentKallmann syndrome gene mutations tested for
propertyPrid  =  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.
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.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
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.
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short nameKMS gene Mut Tested Bld/T

Basic Attributes

classMOLPATH.MUT
type1  Laboratory
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 updated2.67
last change typeNAM  - change to Analyte/Component
change reasonRelease 2.67: COMPONENT: Corrected typo

Related Names

Adhesion molecule-like, X-linked, ADMLX, anosmin 1
Anosmic hypogonadism
Blood
Dysplasia olfactogenitalis of de Morsier
Gene mut tested
Genetics
Heredity
Heritable
HHA
Hypogonadotropic hypogonadism and anosmia
Identity or presence
Inherited
KMS
KMS gene
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Tested
Mutation
Muts
Nominal
PCR
Point in time
Random
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

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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