LOINC Code 94589-9: Hematologic neoplasm chromosome analysis Mate pair sequencing Doc (Bld/BM)
94589-9 is a LOINC code used to identify Hematologic neoplasm chromosome analysis Mate pair sequencing Doc (Bld/BM) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Hematologic neoplasm chromosome analysis. It is commonly used with the system or sample type Bld/Bone mar.
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 Hematologic neoplasm chromosome analysis. It is commonly used with the system or sample type Bld/Bone mar.
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: Mate pair sequencing
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- Hematologic neoplasm chromosome analysis in Blood or Marrow by Mate pair sequencing
- Hematologic neoplasm chromosome analysis
- This term is used for the order & overall chromosome analysis report for identifying hematologic neoplasms in blood or bone marrow specimens by sequencing methods, such as mate pair sequencing. Results may include the overall findings, the result in ISCN format, testing methods, interpretation, recommendations, and references. This is typically second-tier testing when previous cytogenetic studies have detected an acquired chromosome abnormality of unknown significance.
- Bld/Mar; Blood; BM; BON; Bone marrow; Chrom analy; Chromosom; Chromosomes; Cytogenetics; Document; Finding; Findings; Genetics; Hemato; Hematologic chrom analy; Hematology; Heme; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Karyotype; MAR; Marrow (bone); minimal angle of resolution; Minimum angle of resolution; Molecular pathology; MOLPATH; MPSeq; Next generation sequencing; NGS; Oncology; Point in time; Random; WB; Whole blood; Whole blood or Bone marrow
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
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.