94592-3LOINC 2.82
Chromosome rearrangement [Identifier] in Blood or Tissue by Mate pair sequencing Nominal
AML chromo analys Bld/Mar MPSeq
Definition
- This term is used to report the mate pair sequencing results, preferably using a standardize nomenclature such as ISCN, for targeted chromosome analysis of neoplastic clones in blood or bone marrow specimens. Testing is performed in patients with acute myeloid leukemia (AML) or other myeloid malignancies when previous cytogenetic studies are unsuccessful or detect a chromosome abnormality of unknown significance. Results provide diagnostic, prognostic, and therapeutic information for patient care.
Component
- Chromosome rearrangement
Specimen / system
- Bld/Tiss
Class
- MOLPATH
Property
- Prid
Scale
- Nom
Method
- Mate pair sequencing
Related names
- Blood; Chromosom; Chromosomes; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Identity or presence; Inherited; Molecular pathology; MOLPATH; MPSeq; Next generation sequencing; NGS; Nominal; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Chromosom
- Chromosomes
- Genetics
- Heredity
- Heritable
- high-throughput sequencing
- HTS
- Identity or presence
- Inherited
- Molecular pathology
- MOLPATH
- MPSeq
- Next generation sequencing
- NGS
- Nominal
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue