LOINC Code 77128-7: USH1C 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 USH1C 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

• USH1C gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
• USH1C gene mutation analysis limited to known familial mutations
• AIE-75; Blood; DFNB18; DFNB18A; Document; Fam Mut Anl; Finding; Findings; Genetics; harmonin; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; Non-syndromic sensorineural deafness autosomal recessive type 18; NY-CO-37; NY-CO-38; PCR; PDZ-45; PDZ73; PDZ-73; PDZ-73/NY-CO-38; PDZD7C; Point in time; Random; Tissue; Tissue, unspecified; ush1cpst; Usher syndrome 1C (autosomal recessive, severe); Usher syndrome type 1C; 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