Terminology Service for NFDI4Health
JSON

t(16;16)(p13.1;q22)

Go to external page http://purl.obolibrary.org/obo/NCIT_C27759

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

Term info

Label

t(16;16)(p13.1;q22)

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

NCIT_C116977, NCIT_C142800, NCIT_C142799

Display Name

t(16;16)(p13.1;q22)

Legacy Concept Name

t_16_16_p13_q22

Preferred Name

t(16;16)(p13.1;q22)

Semantic Type

Cell or Molecular Dysfunction

UMLS CUI

C2828339

code

C27759