LOINC Code 77118-8: RPGRIP1 gene familial mut analysis Molgen Doc (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 RPGRIP1 gene mutation analysis limited to known familial mutations. 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

• RPGRIP1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
• RPGRIP1 gene mutation analysis limited to known familial mutations
• Blood; Congenital blindness; CORD13; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LCA6; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; PCR; Point in time; Random; Retinitis pigmentosa; retinitis pigmentosa GTPase regulator interacting protein 1; RGI1; RGRIP; RPGRIP; RPGRIP1d; 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