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MedGen UID:
Concept ID:
Cell or Molecular Dysfunction


A cytogenetic abnormality that involves a translocation between chromosomes 11 and 17. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(11;17)

Professional guidelines


Nahi H, Kashif M, Klimkowska M, Karvouni M, Wallblom A, Gran C, Hauenstein J, Frengen N, Gustafsson C, Afram G, Uttervall K, Lund J, Månsson R, Wagner AK, Alici E
Am J Hematol 2021 Aug 1;96(8):925-933. Epub 2021 May 18 doi: 10.1002/ajh.26207. PMID: 33901326
Dorantes-Acosta E, Medina-Sanson A, Jaimes-García Y, López-Martínez B
Rev Invest Clin 2013 Sep-Oct;65(5):392-8. PMID: 24687338
Chen Z, Chen SJ, Wang ZY
C R Acad Sci III 1994 Dec;317(12):1135-41. PMID: 7697468

Recent clinical studies


Courville EL, Shantzer L, Vitzthum von Eckstaedt HC, Mellot H, Keng M, Sen J, Morris A, Williams E, El Chaer F
Lab Med 2022 Jan 6;53(1):95-99. doi: 10.1093/labmed/lmab051. PMID: 34268555

Supplemental Content

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    Practice guidelines

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