What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 77050-3: SUGCT gene familial mut analysis Molgen Doc (Bld/Tiss)

Name: LOINC Code 77050-3: SUGCT gene familial mut analysis Molgen Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:57.647Z

77050-3 is a LOINC code used to identify SUGCT gene familial mut analysis Molgen Doc (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 SUGCT gene mutation analysis limited to known familial mutations. 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 SUGCT gene mutation analysis limited to known familial mutations. 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

SUGCT gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

SUGCT gene mutation analysis limited to known familial mutations

Blood; C7ORF10; chromosome 7 open reading frame 10; DERP13; Document; Fam Mut Anl; Finding; Findings; FLJ11808; Genetics; glutaric aciduria type III; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; ORF19; PCR; Point in time; Random; Retinitis pigmentosa 54; RP 54; Russel-Silver syndrome; succinyl-CoAglutarate-CoA transferase; 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

SUGCT gene familial mut analysis Molgen Doc (Bld/Tiss)SUGCT gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics methodSUGCT Fam Mut Anl Bld/TSUGCT gene mutation analysis limited to known familial mutationsMOLPATH.MUTSUGCT gene familial variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code77050-3

SystemLOINC

Display nameSUGCT gene familial mut analysis Molgen Doc (Bld/Tiss)

DescriptionSUGCT gene mutation analysis limited to known familial mutations

Short nameSUGCT Fam Mut Anl Bld/T

ComponentSUGCT gene mutation analysis limited to known familial mutations

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodMolgen

ClassMOLPATH.MUT

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.52

Last changed2.65

Consumer names

SUGCT gene familial variant analysis, Blood or tissue specimen

Part names

SUGCT gene mutation analysis limited to known familial mutationsFindPtBld/TissDocMolgenFindingPoint 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.