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t(17;21)(q11;q22)

MedGen UID:: 273742
•Concept ID:: C1515730
•: Cell or Molecular Dysfunction

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(17;21)(q11;q22)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Chromosomal translocation
      - t(17;21)(q11;q22)

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