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t(5;17)(q35;q21)

MedGen UID:: 884402
•Concept ID:: C4053814
•: Cell or Molecular Dysfunction

Definition

A chromosomal abnormality consisting of the translocation of 5q32 with 17q21. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(5;17)(q35;q21)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Chromosome 5 Rearrangement
      - t(5;17)(q35;q21)

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