OMOP Concept 40765084
Chromosome analysis copy number change panel by Microarray
StandardMeasurementLOINC62343-9Lab Test
Maps from
0
Descendants
22
Valid from
2 Dec 2010
Valid to
31 Dec 2099
OMOP concepts
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Synonyms
Alternative names recorded for Chromosome analysis copy number change panel by Microarray across source vocabularies.
- arrCGH; Blood; Chrom analy; Chromosom; Chromosomes; CMA # change pnl; Cytogenetics; Exchange; Genetics; Heredity; Heritable; HL7.CYTOGEN; Inherited; Karyotype; No; Num; Pan; PANEL.HL7.CYTOGEN; Panl; Pnl; Point in time; Random; Replace; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
- Chromosome analysis copy number change panel, Blood or tissue specimen
- CMA # change pnl Microarray
- 染色体分析拷贝数变化组套:-:时间点:全血/组织:-:微阵列
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
- 1Chromosome analysis copy number change panel | Blood or Tissue | HL7 cytogenetics panels
- 1Chromosome analysis master panel
- 1HL7 cytogenetics panel
- 2Chromosome analysis master panel | Blood or Tissue | HL7 cytogenetics panels
- 2HL7 cytogenetics panels
- 2Order set
- 3Molecular Pathology Panels
- 4Molecular pathology
- 5Laboratory
- 6{component}
Narrower concepts
(22)Included automatically when you query with descendants.
- 1Chromosome analysis summary panel
- 1Chromosome copy number change panel
- 1Diagnostic impression [Interpretation] in Specimen Narrative
- 1Human reference assembly release, UCSC version [Identifier]
- 1Human reference sequence assembly version
- 1Microarray platform [Identifier] Narrative
- 1Microarray platform version number Narrative
- 1Recommendation [Interpretation] Document
- 1Recommended follow-up [Identifier]
- 1Test performance information in Specimen Narrative
- 2Base pair end coordinate [#]
- 2Base pair start coordinate [#]
- 2Chromosome analysis overall interpretation Qualitative
- 2Chromosome analysis result in ISCN expression
- 2Chromosome band involved end
- 2Chromosome band involved start
- 2Chromosome copy number change [Type]
- 2Flanking normal region after end
- 2Flanking normal region before start
- 2Genetic analysis report
- 2Genetic disease assessed [ID]
- 2Genomic source class [Type]
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