LOINC Code 69963-7: t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript Molgen (BM) [# ratio]
69963-7 is a LOINC code used to identify t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript Molgen (BM) [# ratio] 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 t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript. It is commonly used with the system or sample type 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 t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript. It is commonly used with the system or sample type 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: Molgen
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript [# Ratio] in Bone marrow by Molecular genetics method
- t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript
- ABL; ABL1; ABL1 transcript; ALL; bcr/abl; BCR1; bcr-abl1; BM; BON; Bone marrow; Breakpoint cluster region; Chronic myeloid leukemia; CML; control gene; D22S11; D22S662; DNA; gene fusion; gene translocation; Genetics; Heredity; Heritable; Inherited; JTK7; major breakpoints; MAR; Marrow (bone); Mbr; Mcr; minimal angle of resolution; Minimum angle of resolution; minor breakpoints; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; Number ratio; p150; PCR; Ph chromosome; Philadelphia chromosome; PHL; Point in time; QNT; Quan; Quant; Quantitative; Random; RNA; T prime; t(9,22)(ABL1,BCR) gene translocation; t(9,22)(ABL1,BCR) p190 gene translocation; t(9,22)(ABL1,BCR) Translocation; t(9,22)(q34,q11); t(9,22)(q34.1,q11); t(9;22)(ABL1,BCR); t(ABL1,BCR)e1a2; translocation; v-abl Abelson murine leukemia viral oncogene homolog 1
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.