OMOP Concept 4030176
Chromosome analysis, cytogenetic procedure AND/OR molecular biology method
StandardProcedureSNOMED108261007Procedure
Maps from
4
Descendants
97
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Chromosome analysis, cytogenetic procedure AND/OR molecular biology method via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD9CM | V26.31 | Testing of female for genetic disease carrier status | Non-standard |
| ICD9CM | V26.34 | Testing of male for genetic disease carrier status | Non-standard |
| ICD9CM | V26.39 | Other genetic testing of male | Non-standard |
| Nebraska Lexicon | 108261007 | Chromosome analysis, cytogenetic procedure AND/OR molecular biology method | Non-standard |
Synonyms
Alternative names recorded for Chromosome analysis, cytogenetic procedure AND/OR molecular biology method across source vocabularies.
- análisis cromosómico, procedimiento citogenético Y/O método de biología molecular
- análisis cromosómico, procedimiento citogenético Y/O método de biología molecular (procedimiento)
- Chromosome analysis, cytogenetic procedure AND/OR molecular biology method (procedure)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(97)Included automatically when you query with descendants.
- 170-gene expression profile assay
- 1ADAMTS13 protease molecular detection
- 1Alpha globulin gene analysis
- 1Aneuploidy screening
- 1Breakpoint cluster region analysis
- 1Carrier detection, molecular genetics
- 1Chromosome analysis
- 1Cystic fibrosis carrier detection
- 1Cytogenetic procedure
- 1Detection of Tay Sachs disease carrier status
- 1DNA analysis
- 1DNA hybridization
- 1Duchenne muscular dystrophy carrier detection
- 1Extraction of plasmid deoxyribonucleic acid
- 1Gene expression assay
- 1Genomic deoxyribonucleic acid extraction for mapping
- 1Globin gene analysis
- 1Immunoglobulin gene rearrangement assay
- 1Molecular biology method
- 1N MYC gene amplification
- 1Nucleic acid hybridization procedure
- 1Nucleic acid probe method
- 1T cell receptor gene rearrangement
- 1T cell receptor V-beta analysis
- 1Transmembrane tryptase gene expression analysis
- 2Alpha globulin gene analysis, amniotic fluid
- 2Alpha globulin gene analysis, blood
- 2Breakable chromosome analysis
- 2Breakpoint analysis of deoxyribonucleic acid using fluorescence in situ hybridization
- 2Buccal smear for Barr bodies
- 2Chromosome breakage assay
- 2Chromosome fragility study
- 2Comparative genomic hybridization (cgh) microarray testing for developmental delay, autism spectrum disorder and/or intellectual disability
- 2Cystic fibrosis carrier detection, amniotic fluid
- 2Cystic fibrosis carrier detection, blood
- 2Cystic fibrosis, prenatal detection
- 2DNA analysis, antenatal
- 2DNA hybridization with autoradiography
- 2DNA probe analysis
- 2Duchenne muscular dystrophy carrier detection, amniotic fluid
- 2Duchenne muscular dystrophy carrier detection, blood
- 2Feces-based colorectal cancer DNA screening
- 2Fluorescence in situ hybridization
- 2Gene deletion analysis
- 2Gene expression profiling panel for use in the management of breast cancer treatment
- 2Gene rearrangement analysis
- 2Gene replacement therapy
- 2Genetic screening, molecular method
- 2Hemoglobinopathy DNA studies
- 2Measurement of alpha fetoprotein and analysis of chromosomes in amniotic fluid specimen
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