LOINC Code 94188-0: APC gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
94188-0 is a LOINC code used to identify APC gene del+dup and full mutation 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 APC gene deletion+duplication & full mutation analysis. It is commonly used with the system or sample type Bld/Tiss.
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 APC gene deletion+duplication & 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: Molgen
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- APC gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
- APC gene deletion+duplication & full mutation analysis
- Full gene sequence analysis is performed to detect the presence of a mutation in all coding regions and intron/exon boundaries of the APC gene. In addition, deletion/duplication analysis, such as by array comparative genomic hybridization (aCGH), is used to test for the presence of large deletions or duplications in the APC gene. This test is used to confirm a diagnosis of familial adenomatous polyposis (FAP) for patients with clinical findings.
- Adenomatosis polyposis coli; adenomatous polyposis coli; Adenomatous polyposis of the colon; Amplification; Blood; BTPS2; Del; Del+Dup; Del+Dup + Full Mut Anl; Deletions; Document; Dp; DP2; DP2.5; DP3; Familial adenomatous polyposis; FAP; Finding; Findings; FPC; full gene sequencing; Full Mut Anl; Genetics; GS; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; PCR; Point in time; PPP1R46; 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
Frequently asked questions
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.