Preferred Label : genes;

MeSH definition : A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms.;

MeSH synonym : gene;

MeSH hyponym : genetic materials; Genetic Material; Material, Genetic; Materials, Genetic;

Related MeSH term : cistron; Cistrons;

MeSH annotation : general or unspecified; prefer specifics; restorer genes: index GENES, SUPPRESSOR and probably PLANT INFERTILITY; repressor genes GENES, REGULATOR but also consider REPRESSOR PROTEINS; lac gene LAC OPERON but consider also LAC FACTORS or LAC REPRESSORS (see note on REPRESSOR PROTEINS); split genes EXONS or INTRONS;

Wikipedia link : https://en.wikipedia.org/wiki/Gene;

Details


Main resources

You can consult :

A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms.

https://www.has-sante.fr/jcms/p_3591624/fr/sequencage-haut-debit-cible-des-panels-de-genes-dans-le-diagnostic-des-cardiomyopathies-hereditaires-rapport-d-evaluation
2025
France
health technology assessment
sequence analysis
evaluation studies as topic
diagnosis
genes
sequence determinations
evaluation report
cardiomyopathy, nos
albumin/globulin ratio
no diagnosis
cardiomyopathies

---
https://www.inesss.qc.ca/publications/repertoire-des-publications/publication/principes-et-criteres-permettant-de-baliser-le-recours-au-sequencage-pangenomique-par-rapport-au-sequencage-cible-dun-nombre-limite-de-genes-pour-la-recherche-de-variants-germinaux.html
2024
Canada
technical report
policy
sequence analysis
Limited Lifting Ability
Limited
genes
Has_Target
Criterion
Limited Walking Ability
Number
albumin/globulin ratio
Target
research report
medical futility
principle-based ethics
Ratio
Target Lesion Identification
Regulatory Report
Nucleic Acid Sequencing
sequence determinations

---
http://publications.msss.gouv.qc.ca/msss/document-000179/
2024
false
false
false
false
Canada
French
scientific and technical information
resulting in
genes
physicians
hemoglobinopathies
carrier state, nos
hemoglobinopathy, nos
Handbook
interpreter
Handbook

---
https://www.has-sante.fr/jcms/p_3536022/fr/sequencage-haut-debit-cible-d-un-panel-de-genes-dans-la-prise-en-charge-medicale-des-tumeurs-stromales-gastro-intestinales-rapport-d-evaluation
2024
France
health technology assessment
Panel Device
Regulatory Report
High Level
Digestive System Neoplasm
Charge
sequence determinations
sequence analysis
Physical Examination
Target Lesion Identification
Target
Nucleic Acid Sequencing
intestinal tract, nos
IPSS-R Risk Category High
Topical Route of Administration
genes
High Mitosis-Karyorrhexis Index
Assessment
albumin/globulin ratio
Backflow
IPSS Risk Category High
High-Frequency Microsatellite Instability
Value Above Reference Range
Ratio
evaluation studies as topic
Topical Dosage Form
Evaluation
Assessment
patient care management
evaluation report
gastrointestinal stromal tumors
Has_Target
Output

---
https://www.inesss.qc.ca/publications/repertoire-des-publications/publication/detection-de-la-mutation-d816v-du-gene-kit-par-taan.html
2024
Canada
health technology assessment
KIT Gene
gene, nos
Embarrassment
KIT Gene Mutation
genes
detective
Mutation Detection
KIT NP_000213.1:p.D816V
nucleic acid amplification techniques
Nucleic Acid Amplification Test
mutation

---
https://www.has-sante.fr/jcms/p_3536003/fr/sequencage-haut-debit-cible-d-un-panel-de-genes-dans-la-prise-en-charge-medicale-de-la-leucemie-lymphoide-chronique-rapport-d-evaluation
2024
France
health technology assessment
leukemia, lymphocytic, chronic, B-Cell
IPSS-R Risk Category High
Physical Examination
Has_Target
NCI CTEP SDC Chronic Lymphoid Leukemia Sub-Category Terminology
albumin/globulin ratio
Target
evaluation report
patient care management
sequence analysis
Panel Device
leukemia, lymphoid
Output
High Level
Assessment
Target Lesion Identification
genes
leukaemia
Topical Dosage Form
Assessment
sequence determinations
chronic lymphocytic leukemia
IPSS Risk Category High
High Mitosis-Karyorrhexis Index
Topical Route of Administration
Evaluation
Charge
Ratio
Backflow
Chronic Lymphocytic Leukemia
High-Frequency Microsatellite Instability
Regulatory Report
Value Above Reference Range
evaluation studies as topic
Nucleic Acid Sequencing

---
https://www.has-sante.fr/jcms/p_3535386/fr/sequencage-haut-debit-cible-d-un-panel-de-genes-dans-la-prise-en-charge-medicale-du-cancer-du-poumon-recherche-des-alterations-moleculaires-somatiques
2024
France
health technology assessment
Impairment
IPSS Risk Category High
lung neoplasms
sequence determinations
Has_Target
Nucleic Acid Sequencing
Topical Route of Administration
Output
Value Above Reference Range
Cancer Research
Lung Carcinoma
neoplasm, malignant
Cancer Burden
medical research
Backflow
Somatic
Topical Dosage Form
Molecular
genes
Panel Device
IPSS-R Risk Category High
biomedical research
High-Frequency Microsatellite Instability
Alteration
Target
lung cancer
sequence analysis
High Level
High Mitosis-Karyorrhexis Index
Target Lesion Identification
patient care management

---
https://cps.ca/fr/documents/position/pharmacotherapie-genes-medicaments-psychoactifs
2024
Canada
practice guideline
genes
Adolescents
Gene
Offspring
adolescent
drug, nos
Nutritional Support
Pharmacotherapy
Medication
Pharmacologic Substance
adolescence
child, nos
child
Child
Mathematical Operator
drug therapy
pharmaceutical preparations
Teenager
Drug Therapy
GDC Therapeutic Agent Terminology
Adolescent

---
https://www.inesss.qc.ca/publications/repertoire-des-publications/publication/principes-et-criteres-de-selection-des-genes-pour-le-diagnostic-moleculaire-des-maladies-en-genetique-constitutionnelle-par-sequencage-de-nouvelle-generation-sng.html
2023
Canada
technical report
Molecular genetics
policy
disease
family characteristics
generations
genetics, molecular
genetic selection
Genetic disease
principle-based ethics
nasogastric tube
pathology, molecular
Diseases
no diagnosis
selection, genetic
selection criteria
hereditary disease, nos
sequence analysis
genetic diseases, inborn
diagnosis
Molecular genetics
genes
patient selection
sequence determinations

---
https://cps.ca/fr/documents/position/la-pharmacotherapie-en-fonction-des-genes-chez-les-enfants
2023
false
false
false
false
false
Canada
pharmacogenetics
Drug-Related side effects and adverse reactions
practice guideline
child
genes

---
https://www.has-sante.fr/jcms/p_3390116/fr/synaptopathie-due-aux-variations-pathogenes-du-gene-otof
2022
France
practice guideline
genetic variation
chronic disease
Chronic disease
gene, nos
Diseases
Embarrassment
Handbook
chronic disease, nos
genes
variant

---
https://www.has-sante.fr/jcms/p_3356304/fr/detection-d-alterations-du-gene-ret-par-la-technique-de-sequencage-nouvelle-generation-ngs-cancer-bronchique-non-a-petites-cellules-et-cancer-medullaire-de-la-thyroide
2022
France
health technology assessment
thyroid neoplasms
thyroid cancer, medullary
Thyroid cancer
malignant neoplasm thyroid
neoplasm, malignant
Techniques
carcinoma, non-small-cell lung
detective
thyroid carcinoma
cells
bronchus, nos
"u" lymphocyte
Embarrassment
gene, nos
generations
sequence analysis
due to
Techniques
sequence determinations
bone marrow cells
Techniques
Techniques
Cell
family characteristics
thyroiditis, nos
genes

---
https://www.inrs.fr/media.html?refINRS=outil62
2021
France
questionnaires
software
tool, nos
questionnaires
Surveys and Questionnaires
gene, nos
Acoustics
Embarrassment
genes
acoustics

---
https://www.inrs.fr/media.html?refINRS=ED%206402
2021
France
technical report
genes
gait
environment
Embarrassment
evaluation studies as topic
gait, nos
Environment
gene, nos
environment

---
https://www.cochrane.org/fr/CD012894/interventions-visant-ameliorer-le-bien-etre-psychosocial-des-femmes-presentant-une-mutation-du-gene
2019
France
United Kingdom
review of literature
french abstract
risk reduction
Psychosocial Support Systems
operative procedure, nos
risk reduction behavior
women
surgical procedures, operative
Embarrassment
genes
gene, nos
procedural approach, nos
female
mutation
women
female

---
https://tel.archives-ouvertes.fr/tel-02866730
2019
France
dissertations, academic
Identification, Psychological
genes
Diseases
Inflammatory disease
disease
disease, nos
De-Identification
patient participation
disease
Data Anonymization

---
http://www.theses.fr/2019NORMC418
2019
France
dissertations, academic
attention
genes, neoplasm
computational biology
genes
Applications
Applications
ovary
breast
Bio-Informatics
disease susceptibility
Applications
tool, nos
genes

---
http://www.theses.fr/2018SACLS591
2018
France
dissertations, academic
genes
malignant neoplasm prostate
risk
neoplasm, malignant
work
prostatic neoplasms
circadian rhythm
Prostate cancer
occupation, nos
prostate, nos
Night Shift Work
Labor ; manpower ; population
night time
circadian rhythm, nos
prostate cancer
role
prostatism, nos

---
https://anpgm.fr/media/documents/anpgm_135-deficits_constitutionnels_rares_en_facteurs_de_coagulation.pdf
2018
France
guideline
hemophilia b, nos
coagulation factor, nos
Hemophilia B
blood coagulation disorder, nos
genes
coagulants
hemophilia B
von willebrand diseases
von willebrand factor
Rare disease
Coagulation factors
rare diseases
Diseases
coagulants

---
https://anpgm.fr/media/documents/anpgm_133__hyperplasie-congenitale-surrenales_cyp21a2_hors_ngs.pdf
2018
France
guideline
congenital adrenal cortical hyperplasia, nos
gene, nos
congenital adrenal hyperplasia due to 21 hydroxylase deficiency
genes
Embarrassment
steroid 21-hydroxylase
adrenal hyperplasia, congenital
data collection
Acanthosis
Hyperplasia
steroid 21-monooxygenase deficiency, simple virilizing type

---
https://www.franceculture.fr/emissions/la-methode-scientifique/epigenetique-quand-le-pouvoir-des-genes-atteint-ses-limites
2017
false
false
false
France
French
radio broadcast
genes
medical futility
marginal
borderline
involved
epigenetics
epigenomics

---
http://www.hcsp.fr/explore.cgi/avisrapportsdomaine?clefr=589
http://www.hcsp.fr/explore.cgi/avisrapportsdomaine?clefr=620
2016
false
false
false
France
French
scientific and technical information
gene, nos
enterobacteriaceae
resistant
diffuse rigidity
colistin
no diagnosis
genes
diagnosis
colistin
microbiology
carbapenemase
microbiology
bacterial proteins
beta-Lactamases

---
https://www.nek-cne.admin.ch/inhalte/Themen/Stellungnahmen/fr/NEK_Kurzstellungnahme_FR_korr.pdf
2016
false
false
false
France
French
scientific and technical information
human gene, nos
embryo
humans
genes
embryonic structures

---
https://anpgm.fr/media/documents/ANPGM_080-v2-Hemophilie.pdf
2016
France
guideline
Hemophilia B
hemophilia B
genes
hemophilia b, nos

---
https://anpgm.fr/media/documents/ANPGM_074-v3-CFTR.pdf
2016
France
guideline
Embarrassment
genes
best practices
Practice
gene, nos
cystic fibrosis transmembrane conductance regulator
practice guidelines as topic

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=2163
false
true
false
France
scientific and technical information
syndrome
Cohen syndrome
genoa syndrome
cohen syndrome
craniosynostoses
craniosynostoses
Genoa syndrome
holoprosencephaly
genes

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=99974
2011
France
scientific and technical information
genes
immunoglobulin a deficiency 2
iga deficiency

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=88924
2011
France
scientific and technical information
Genoa syndrome
genes
sclerosis
syndrome
polycystic kidney, type 1 autosomal dominant disease
polycystic kidney, autosomal dominant

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=99764
2011
France
scientific and technical information
hypoaldosteronism
Cytochrome P-450 CYP11B2
genes

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=98912
2011
France
scientific and technical information
muscular diseases
mutation
myopathy, myofibrillar, Zasp-Related
myopathy, myofibrillar, Zasp-Related
genes

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=101069
2011
France
scientific and technical information
corneal dystrophies, hereditary
genes

---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=137634
2011
France
scientific and technical information
syndrome
growth disorders
Learning Disabilities
genes
Genoa syndrome

---
https://anpgm.fr/media/documents/ANPGM_041_Dystrophie_retiniennes_gne_RDS.doc
2010
France
guideline
Embarrassment
retinal dystrophies
genes
dystrophy, nos
mutation
Dystrophy
gene, nos
retina, nos

---
https://smf.swisshealthweb.ch/fr/article/doi/fms.2010.07046/
2010
false
false
false
Switzerland
journal article
genes
genets
financial support
genetics
science

---
https://anpgm.fr/media/documents/ANPGM_039_Stargardt_ABCA4.doc
2010
France
guideline
disease
gene, nos
Diseases
stargardt's disease
genes
Diseases Category
Embarrassment
Disease
disease

---
https://anpgm.fr/media/documents/ANPGM_059_RM_et_gne_GDI1_Xq28.doc
2009
France
guideline
genes
deficiency, mental
Genetics
Embarrassment
Genetics
abnormal mental state
gene, nos
intellectual disability
genetic linkage
Genetics
non-specific

---
https://anpgm.fr/media/documents/ANPGM_053_RM_li_au_gne_Oligophrnine.doc
2009
France
guideline
mental retardation
intellectual disability
Embarrassment
genes
mental retardation, nos
linked gene

---
https://anpgm.fr/media/documents/ANPGM_052_Lissencephalie_LIS1_et_DCX.doc
2009
France
guideline
genes
lissencephaly
Lissencephaly
linked gene

---
https://anpgm.fr/media/documents/ANPGM_015_Maladie_dAlexander.doc
2009
France
guideline
gene, nos
alexander's disease
Embarrassment
glial fibrillary acidic protein
Alexander disease
Diseases
genes
alexander disease

---
https://anpgm.fr/media/documents/ANPGM_060_Syndrome_de_Nance-Horan_NHS.doc
2009
France
guideline
genoa syndrome
Nance-Horan syndrome
Embarrassment
genes
gene, nos
craniosynostoses
holoprosencephaly
cataract
tooth abnormalities
genetic diseases, X-linked

---
https://anpgm.fr/media/documents/ANPGM_014_Megalencephalie_et_leucodystrophie_MLC1.doc
2009
France
guideline
cysts
gene, nos
megalencephalic leukoencephalopathy with subcortical cysts
Leukodystrophy
genes
leukodystrophy, nos
Megalencephaly
macroencephaly
Megalencephaly
Embarrassment
hereditary central nervous system demyelinating diseases

---
https://smf.swisshealthweb.ch/fr/article/doi/fms.2009.06930/
2009
false
true
false
Switzerland
osteoporosis
journal article
osteoporosis
genes

---
http://atlasgeneticsoncology.org/Educ/GenHemoglobID30014FS.html
2008
false
true
false
France
educational course
globins
thalassemia
hemoglobin s disease
anemia, sickle cell
alpha-Thalassemia
genes

---
http://www.has-sante.fr/portail/display.jsp?id=c_272448
2005
true
false
Haute Autorité de santé
France
French
french abstract
obsessive-compulsive disorder
obsessive-compulsive disorder
prevalence
bibliography of medicine
twins
genes
obsessive-compulsive disorder
obsessive-compulsive disorder
diagnostic imaging
meta-analysis as topic
treatment outcome
obsessive-compulsive disorder
international classification of diseases
diagnosis, differential
psychiatric status rating scales
Cognitive Behavioral Therapy
psychotherapy
Selective Serotonin Reuptake Inhibitors
clomipramine
drug combinations
combined modality therapy
obsessive-compulsive disorder
psychosurgery
internal capsule
gyrus cinguli
caudate nucleus
limbic system
psychosurgery
psychosurgery
deep brain stimulation
clinical protocols
obsessive behavior
obsessive-compulsive disorder
obsessive-compulsive disorder
comorbidity
Self-Assessment
obsessive-compulsive disorder
drug resistance
child
adolescent
diseases in twins
patient care management
health technology assessment
obsessive-compulsive disorder

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26/04/2025


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