Chromosome 12 Trisomy and Chromosome Region 11q22.3 and 13q14 and 17p13.1 Deletion in Blood or Tissue by FISH

Preferred Label : Chromosome 12 Trisomy and Chromosome Region 11q22.3 and 13q14 and 17p13.1 Deletion in Blood or Tissue by FISH;

NCIt definition : A fluorescent in situ hybridization-based procedure that detects chromosome 12 trisomy and/or deletions in chromosome regions 11q22.3, 13q14 and/or 17p13.1 in a blood or tissue specimen.;

NCI Metathesaurus CUI : CL1914254;

Codes from synonyms : 82256-9;

Details

Origin ID

C193890;

UMLS CUI

C5782084;

Semantic type(s)
- Laboratory Procedure [UMLS semantic type]
concept_is_in_subset
- mCode Terminology [NCIt concept]
- mCode Tumor Marker Test Value Set [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