LOINC Code 42785-6: FGFR1 gene targeted mutation analysis Molgen Nom (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 FGFR1 gene targeted 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

• FGFR1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
• FGFR1 gene targeted mutation analysis
• Basic fibroblast growth factor receptor 1 precursor; BFGFR; bFGF-R-1; Blood; CD331; CEK; C-FGR; FGFBR; FGFR-1; fibroblast growth factor receptor 1; fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome); FLG; FLT2; FLT-2; Genetics; H2; H3; H4; H5; HBGFR; Heredity; Heritable; HH2; HRTFDS; Identity or presence; Inherited; KAL2; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; N-SAM; OGD; PCR; Point in time; Random; 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