del(17p13)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A deletion of chromosomal material at 17p13. This chromosomal aberration includes deletion of the TP53 gene and is associated with multiple myeloma, chronic lymphocytic leukemia, acute myeloid leukemia and myelodysplastic syndrome.

**Synonyms:** - -17p13 - 17p13 Deletion - del(17)(p13)