AutoICD API

21701-8

Laboratory

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

LOINC 6-Axis Classification

Component

Kallmann syndrome gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

KMS gene Mut Tested Bld/T

Display Name

Kallmann syndrome gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

Adhesion molecule-like, X-linked, ADMLX, anosmin 1Anosmic hypogonadismBloodDysplasia olfactogenitalis of de MorsierGene mut testedGeneticsHeredityHeritableHHAHypogonadotropic hypogonadism and anosmiaIdentity or presenceInheritedKMSKMS geneMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21701-8?

LOINC code 21701-8 identifies "Kallmann syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures Kallmann syndrome gene mutations tested for in Bld/Tiss.

What does 21701-8 measure?

This code measures Kallmann syndrome gene mutations tested for in Bld/Tiss. It belongs to the MOLPATH.MUT class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.