LOINC Code 103734-0: Dyserythropoietic anemia multigene analysis Sequencing Doc (Specimen)

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 Dyserythropoietic anemia multigene analysis. It is commonly used with the system or sample type XXX.

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

• Dyserythropoietic anemia multigene analysis in Specimen by Sequencing
• Dyserythropoietic anemia multigene analysis
• This profile evaluates for hereditary (congenital) causes of dyserythropoietic anemia
• Document; Finding; Findings; Gene; Gene panel; high-throughput sequencing; HTS; Misc; Miscellaneous; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; Next generation sequencing; NGS; Other; Point in time; Random; Spec; To be specified in another part of the message; Unspecified

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