LP19829-8
t(1;19)(q23.3;p13.3)(PBX1,TCF3)
Active
Description
Chromosomal translocation t(1;19)(q23.3;p13.3) PBX1/TCF3 is caused by a breakpoint in 19p13.3 and occurs in two different forms: 1) a balanced form found in one fourth of cases with a der(1) and a der(19) and 2) an unbalanced form found in 3/4 cases with 2 normal chromosomes 1, a der(19), and 1 normal chromosome 19. This translocation is mostly found in acute lymphoblastic leukemia (ALL), L1/L2 type, as well as L3-like ALL, T-lineage ALL (T-ALL), non-Hodgkin lymphomas (NHL), and acute myeloid leukemias (AML).[Atlas Genetics Oncology:t0119ID1048] Source: Regenstrief LOINC, t(1;19)(q23;p13) TCF3/PBX1
Basic Part Properties
- Part Display Name
- t(1;19)(q23.3;p13.3)(PBX1,TCF3)
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2000-05-04
- Construct for LOINC Short Name
- t(1;19)(PBX1,TCF3)
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | t(1; Synonyms: T(1,19)(PBX1,TCF3) 基因易位; |
| et-EE | Estonian (Estonia) | t(1,19)(PBX1,TCF3) translokatsioon |
| es-ES | Spanish (Spain) | t(1; |
| it-IT | Italian (Italy) | t(1; |
| tr-TR | Turkish (Turkey) | t(1; |
| ru-RU | Russian (Russian Federation) | t(1; |
| nl-NL | Dutch (Netherlands) | t(1; |
| fr-CA | French (Canada) | t(1; |
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