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t(9;17)(q22;q11)

MedGen UID:: 273761
•Concept ID:: C1515806
•: Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the NR4A3 gene on chromosome 9q31 and the TAF15 gene on chromosome 17q12. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(9;17)(q22;q11)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosome 17 disorder
    - t(9;17)(q22;q11)

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