LOINC Code 94212-8: PKLR gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
94212-8 is a LOINC code used to identify PKLR 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 PKLR 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 PKLR 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
- PKLR gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
- PKLR gene deletion+duplication & full mutation analysis
- Test includes full sequence analysis (e.g. by Sanger and/or next-generation sequencing) and deletion/duplication analysis for the detection of variants and large deletions/duplications in the PKLR gene in patients with low levels of erythrocytic PK enzymatic activity. Testing is performed to aid in the diagnosis of pyruvate kinase (PK) deficiency.
- Amplification; Blood; Del; Del+Dup; Del+Dup + Full Mut Anl; Deletions; Document; Dp; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; PCR; PK1; PKL; PKR; PKRL; Point in time; Pyruvate kinase 1 gene; Pyruvate kinase isozymes R/L gene; pyruvate kinase, liver and RBC; Pyruvate kinase, liver and RBC gene; Random; Red cell/liver pyruvate kinase gene; RPK; R-type/L-type pyruvate kinase gene; 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.