Terminology Service for NFDI4Health
t(9;22)
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http://purl.obolibrary.org/obo/NCIT_C117116
A translocation between chromosome 9 and chromosome 22 that may be associated with Philadelphia chromosome and increased susceptibility to several types of leukemia. [ ]
Term info
Label
t(9;22)
Synonyms
- t(9;22)
Subsets
NCIT_C156953, NCIT_C156952, NCIT_C116977, NCIT_C159339, NCIT_C142800, NCIT_C142799
Contributing Source
CTRP, CPTAC
Display Name
t(9;22)
Preferred Name
t(9;22)
Semantic Type
Cell or Molecular Dysfunction
UMLS CUI
C3897138
code
C117116