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 94207-8: MMADHC gene full mutation analysis Sequencing Doc (Bld/Tiss)

Name: LOINC Code 94207-8: MMADHC gene full mutation analysis Sequencing Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:23.055Z

94207-8 is a LOINC code used to identify MMADHC gene full mutation analysis Sequencing 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 MMADHC gene full mutation analysis. 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 MMADHC gene full mutation analysis. 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: Sequencing

What it does not mean

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

Key facts

MMADHC gene full mutation analysis in Blood or Tissue by Sequencing

MMADHC gene full mutation analysis

Full gene sequence analysis to identify a mutation in the coding regions and intron/exon boundaries of the MMADHC gene. Testing may be performed for the diagnosis of methylmalonic acidemia with homocystinuria (type cblD).[GHR geneMMADHC]

Blood; C2orf25; cblD; CL25022; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; metabolism of cobalamin associated D; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; Point in time; Random; sequencing of entire coding region; 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

MMADHC gene full mutation analysis Sequencing Doc (Bld/Tiss)MMADHC gene full mutation analysis in Blood or Tissue by SequencingMMADHC Full Mut Anl Bld/T SeqMMADHC gene full mutation analysisMOLPATHMMADHC gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code94207-8

SystemLOINC

Display nameMMADHC gene full mutation analysis Sequencing Doc (Bld/Tiss)

DescriptionMMADHC gene full mutation analysis

Short nameMMADHC Full Mut Anl Bld/T Seq

ComponentMMADHC gene full mutation analysis

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodSequencing

ClassMOLPATH

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.68

Last changed2.68

Consumer names

MMADHC gene variant analysis, Blood or tissue specimen

Part names

MMADHC gene full mutation analysisFindPtBld/TissDocSequencingFindingPoint in time (spot)Blood or Tissue

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.