t(9;22)(q22-23;q11-12)

Preferred Label : t(9;22)(q22-23;q11-12);

NCIt definition : A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (within q22-23) of chromosome 9 and the long arm (within q11-12) of chromosome 22.;

NCI Metathesaurus CUI : CL1906512;

Details

Origin ID

C199603;

cytogenetic_abnormality_involves_chromosome
- Human Chromosome 22 [NCIt concept]
- Human Chromosome 9 [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients