Preferred Label : chromosome analysis, nos;
Origin ID : P3-49000;
UMLS CUI : C0200867;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- SNOMED CT concept
- Semantic type(s)
- UMLS correspondences (same concept)
http://www.eaclf.org/docs/TestADNlc-Notice_final.pdf
2024
France
patient education handout
Last Screening
information dissemination
pregnancy, nos
Destination
Circulating Cell-Free DNA
emigration and immigration
Informative
mass screening
Screening Study
Cytogenetic Abnormality
Substance Screening
Chromosome Disorder
Cell-Free DNA Blood Collection Tube
dna analysis, nos
DNA Analysis
chromosomal disease, nos
cfDNA Mutation
Informed
Pregnant People
DNA
Gravida
Genetic Screening
Cell-Free Nucleic Acids
Human Cells, Tissues, and Cellular and Tissue-Based Products Screening
chromosome analysis, nos
Cancer Screening
Trial Screening
Eligibility Determination
Site Screening
No Information Available
screening
chromosomes
chromosome aberrations
Oprelvekin
---
https://www.has-sante.fr/jcms/p_3453213/fr/analyse-chromosomique-sur-puce-a-adn-acpa-en-contexte-postnatal
2023
France
evaluation of the transparency committee
oligonucleotide array sequence analysis
flea, nos
DNA
Technology
technology assessment
chromosome analysis, nos
chromosomes
health
technology assessment, biomedical
dna analysis, nos
---
