LOINC Code 85383-8: EGFR gene c.2369C>T actual/normal Molgen (cfDNA) [Relative ratio]
85383-8 is a LOINC code used to identify EGFR gene c.2369C>T actual/normal Molgen (cfDNA) [Relative ratio] 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 EGFR gene.c.2369C>T actual/normal. It is commonly used with the system or sample type Plas.cfDNA.
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 EGFR gene.c.2369C>T actual/normal. It is commonly used with the system or sample type Plas.cfDNA.
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
- EGFR gene c.2369C>T actual/normal in Plasma cell-free DNA by Molecular genetics method
- EGFR gene.c.2369C>T actual/normal
- The EGFR gene mutation c.2369C>T leads to a mutation that interferes with the treatment of patients with non-small cell lung cancer. The mutation is detected in the plasma as free floating cell-free DNA and is present in 50-60% of patients resistant to treatment with first and second generation tyrosine kinase inhibitors.
- Act/Nor; Control; EGFR c.2369C>T; epidermal growth factor receptor; Epidermal growth factor receptor gene; ERBB; ERBB1; Genetics; HER1; Heredity; Heritable; Inherited; mENA; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; NISBD2; Oncogene ERBB; PCR; PIG61; Pl; Plasma; Plsm; Point in time; QNT; Quan; Quant; Quantitative; Random; Relative ratio; rs121434569; T prime; T790M; Thr790Met; V-ERB-B avian erythroblastic leukemia viral oncogene homolog
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.