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del(3p13-14)

MedGen UID:: 1662172
•Concept ID:: C4744443
•: Cell or Molecular Dysfunction

Synonym:

del(3)(p13;p14)

Definition

A cytogenetic abnormality that refers to deletion of chromosome bands 13-14 on the short arm of chromosome 3. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVdel(3p13-14)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Chromosomal Deletion
      - del(3p13-14)

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