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inv(16)(p13.1;q22)

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A chromosomal inversion that involves chromosome 16. It is associated with the development of acute myeloid leukemia CBFB-MYH11, acute myelomonocytic leukemia with abnormal eosinophils, and granulocytic sarcoma. [ ]

Term info

Label

inv(16)(p13.1;q22)

Synonyms
  • inv(16)(p13.1;q22)
  • inv(16)(p13;q22)
  • inv(16)(p13q22)
Subsets

NCIT_C116977, NCIT_C142800, NCIT_C142799

Display Name

inv(16)(p13.1;q22)

Legacy Concept Name

inv_16_p13_q22

Preferred Name

inv(16)(p13.1;q22)

Semantic Type

Cell or Molecular Dysfunction

UMLS CUI

C3897145

code

C36373