LOINC Code 76032-2: SGSH gene full mutation analysis Sequencing 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 SGSH gene 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: Sequencing

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• SGSH gene full mutation analysis in Blood or Tissue by Sequencing
• SGSH gene full mutation analysis
• Blood; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HSS; HTS; Human N-sulphoglucosamine sulphohydrolase mRNA, complete cds; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MPS3A; Mut; Mutations; Next generation sequencing; NGS; N-sulfoglucosamine sulfohydrolase; N-sulfoglucosamine sulfohydrolase (sulfamidase); Point in time; Random; sequencing of entire coding region; SFMD; Sulfoglucosamine sulfamidase gene; Sulphamidase gene; 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