About: B Acute Lymphoblastic Leukemia with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • B Acute Lymphoblastic Leukemia with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)
equivalentClass
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • B Acute Lymphoblastic Leukemia with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)
UMLS_CUI
  • C2698305
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • B_Acute_Lymphoblastic_Leukemia_with_t_12_21_p13_q22_TEL-AML1_ETV6-RUNX1
FULL_SYN
  • B-Cell Acute Lymphoblastic Leukemia with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)SYNCI
  • B Acute Lymphoblastic Leukemia with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)PTNCI
  • B-Acute Lymphoblastic Leukemia with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)SYNCI
DEFINITION
  • A B-cell acute leukemia characterized by the presence of lymphoblasts that carry a translocation between the TEL gene on chromosome 12 and the AML1 gene on chromosome 21. It results in the production of the TEL-AML1 (ETV6-RUNX1) fusion protein. It is commonly seen in children and rarely in adults. It has a favorable clinical outcome.NCI
code
  • C80343
is someValuesFrom of
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