LOINCActiveBoth

LOINC Code 53792-8: PTPN11 gene mutations tier 3 Molgen Nom (Bld/Tiss)

53792-8 is a LOINC code used to identify PTPN11 gene mutations tier 3 Molgen Nom (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component PTPN11 gene targeted mutation analysis.tier 3. It is commonly used with the system or sample type Bld/Tiss.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component PTPN11 gene targeted mutation analysis.tier 3. It is commonly used with the system or sample type Bld/Tiss.

When is it used?

  • Used in lab systems, EHRs, and clinical data exchange.
  • May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
  • Status: ACTIVE
  • Order vs observation: Both
  • Method: Molgen

What it does not mean

  • The code identifies the observation or test, not the actual result.

Key facts

PTPN11 gene mutations tier 3 found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
PTPN11 gene targeted mutation analysis.tier 3
Blood; BPTP3; CFC; Genetics; Heredity; Heritable; HGNC8012; Identity or presence; III; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mut Anl tier3; Mutations; Nominal; Noonan syndrome 1; NS1; PCR; Point in time; protein tyrosine phosphatase, non-receptor type 11; protein tyrosine phosphatase, non-receptor type 11 gene; PTP-1D; PTP2C; Random; SHP2; SHP-2; SHPTP2; SH-PTP2; SH-PTP3; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

PTPN11 gene mutations tier 3 Molgen Nom (Bld/Tiss)PTPN11 gene mutations tier 3 found [Identifier] in Blood or Tissue by Molecular genetics method NominalPTPN11 gene Mut Anl tier3 Bld/TPTPN11 gene targeted mutation analysis.tier 3MOLPATH.MUTPTPN11 gene tier 3 variant analysis, Blood or tissue specimenPrid

Frequently asked questions

Code details

Code53792-8
SystemLOINC
Display namePTPN11 gene mutations tier 3 Molgen Nom (Bld/Tiss)
DescriptionPTPN11 gene targeted mutation analysis.tier 3
Short namePTPN11 gene Mut Anl tier3 Bld/T
ComponentPTPN11 gene targeted mutation analysis.tier 3
PropertyPrid
TimingPt
System (specimen)Bld/Tiss
ScaleNom
MethodMolgen
ClassMOLPATH.MUT
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.26
Last changed2.63

Consumer names

PTPN11 gene tier 3 variant analysis, Blood or tissue specimen

Part names

PTPN11 gene targeted mutation analysis.tier 3PridPtBld/TissNomMolgenPresence or IdentityPoint in time (spot)Blood or TissueMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.

LOINC Code 53792-8 | HealthAssure