Frequency genetic predisposition to disease. Medical search. Frequent questions

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Anatomy9

Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 7 Brain Adipose Tissue Intestinal Mucosa Cells, Cultured Neurons Lymphocytes

Organisms5

Mice, Inbred Strains Mice, Inbred C57BL Mice, Transgenic Mice, Knockout Mice, Inbred BALB C

Diseases55

Genetic Predisposition to Disease Disease Susceptibility Neoplastic Syndromes, Hereditary Disease Models, Animal Obesity Diabetes Mellitus, Type 2 Diseases in Twins Neoplasms Neoplasms, Multiple Primary Autoimmune Diseases Breast Neoplasms Neoplasms, Second Primary Syndrome Hypertension Thyroiditis, Autoimmune Liver Cirrhosis, Biliary Crohn Disease Diabetes Mellitus, Type 1 Celiac Disease Chromosome Aberrations Skin Neoplasms Diabetic Nephropathies Alcoholism Disease Progression Lupus Erythematosus, Systemic Sjogren's Syndrome Colitis, Ulcerative Bloom Syndrome Colorectal Neoplasms Body Weight Inflammation Inflammatory Bowel Diseases Li-Fraumeni Syndrome Fanconi Anemia Lung Neoplasms Adenocarcinoma Cardiovascular Diseases Ataxia Telangiectasia Adenomatous Polyposis Coli Asthma Colorectal Neoplasms, Hereditary Nonpolyposis Rothmund-Thomson Syndrome Insulin Resistance Peutz-Jeghers Syndrome Genomic Instability Nijmegen Breakage Syndrome Werner Syndrome Neurofibromatoses Beckwith-Wiedemann Syndrome Basal Cell Nevus Syndrome Neurofibromatosis 1 Hereditary Breast and Ovarian Cancer Syndrome Retinoblastoma Ovarian Neoplasms Wilms Tumor

Chemicals and Drugs38

Genetic Markers HLA-DQ Antigens HLA-DQ beta-Chains HLA-DRB1 Chains Autoantibodies HLA Antigens HLA-DR Antigens Peptidyl-Dipeptidase A DNA DNA-Binding Proteins RecQ Helicases Carcinogens Proteins Biological Markers Ethanol Carrier Proteins Cytokines RNA, Messenger BRCA2 Protein Tumor Necrosis Factor-alpha Blood Glucose Insulin Tumor Suppressor Proteins DNA, Neoplasm MutS Homolog 2 Protein BRCA1 Protein DNA Helicases Fanconi Anemia Complementation Group Proteins Ataxia Telangiectasia Mutated Proteins HLA-DR Serological Subtypes Nuclear Proteins DNA Primers Protein-Serine-Threonine Kinases Neoplasm Proteins Cell Cycle Proteins Mutagens Fanconi Anemia Complementation Group C Protein DNA Repair Enzymes

Analytical, Diagnostic and Therapeutic Techniques and Equipment48

Pedigree Case-Control Studies Risk Factors Genetic Testing Pelvimetry Chromosome Mapping Genetic Association Studies DNA Mutational Analysis Disease Models, Animal Genome-Wide Association Study Obesity Cohort Studies Polymerase Chain Reaction Incidence Odds Ratio Risk Prevalence Risk Assessment Body Mass Index Models, Genetic Crosses, Genetic Prospective Studies Chi-Square Distribution Sequence Analysis, DNA Models, Biological Logistic Models Analysis of Variance Reference Values Questionnaires Body Weight Retrospective Studies Gene Expression Profiling Severity of Illness Index Prognosis Regression Analysis Follow-Up Studies Blood Pressure Oligonucleotide Array Sequence Analysis Magnetic Resonance Imaging Longitudinal Studies Registries Acoustic Stimulation Electric Stimulation Heterozygote Detection Micronucleus Tests Electroencephalography Reproducibility of Results Fourier Analysis

Psychiatry and Psychology11

Family Smoking Schizophrenia Siblings Alcoholism Life Style Anxiety Stress, Psychological Motor Activity Alcohol Drinking Auditory Threshold

Phenomena and Processes82

Genetic Predisposition to Disease Gene Frequency Genotype Polymorphism, Genetic Alleles Polymorphism, Single Nucleotide Germ-Line Mutation Disease Susceptibility Phenotype Haplotypes Mutation Genetic Markers Genetic Linkage Gene-Environment Interaction Genetic Variation Heredity Linkage Disequilibrium Heterozygote Obesity Penetrance Microsatellite Repeats Genetic Loci Time Factors Genes, BRCA1 Homozygote Environment Base Sequence Polymorphism, Single-Stranded Conformational Pregnancy Polymorphism, Restriction Fragment Length Odds Ratio Risk Inheritance Patterns Body Mass Index Autoimmunity Chromosomes, Human, Pair 2 Lod Score Chromosomes, Human, Pair 6 Species Specificity Diet Exons Chi-Square Distribution Chromosome Aberrations Promoter Regions, Genetic Chromosomes, Human, Pair 7 Genome, Human Quantitative Trait Loci Aging Body Weight Motor Activity Epigenesis, Genetic DNA Repair Immunity, Innate Signal Transduction Blood Pressure Homeostasis Gene Expression Regulation Gene Expression Recombination, Genetic Insulin Resistance Mutation, Missense Genes, BRCA2 DNA Damage Vibration Loss of Heterozygosity Gene Deletion Genomic Instability Point Mutation Action Potentials Genes, Tumor Suppressor Genes, p53 Frameshift Mutation Periodicity Sex Characteristics Base Pair Mismatch DNA Mismatch Repair Genetic Heterogeneity Amino Acid Sequence Sound Exome Sister Chromatid Exchange Fourier Analysis

Disciplines and Occupations2

Genetics, Population Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Family Siblings

Information Science8

Incidence Base Sequence Prevalence Molecular Sequence Data Questionnaires Registries Amino Acid Sequence Fourier Analysis

Named Groups9

Twins, Monozygotic Asian Continental Ancestry Group European Continental Ancestry Group Infant, Newborn Siblings Twins, Dizygotic African Continental Ancestry Group African Americans Jews

Health Care31

Case-Control Studies Risk Factors Genetic Testing Family Health Age of Onset Genome-Wide Association Study Cohort Studies Age Factors Incidence Environment Causality Odds Ratio Risk Prevalence Risk Assessment Body Mass Index Sex Factors Prospective Studies Chi-Square Distribution Environmental Exposure Logistic Models Analysis of Variance Questionnaires Retrospective Studies Severity of Illness Index Regression Analysis Follow-Up Studies Longitudinal Studies Registries Genetic Counseling Reproducibility of Results

Geographicals8

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Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Genetic Predisposition to Disease Gene Frequency Genotype Polymorphism, Genetic Alleles Polymorphism, Single Nucleotide Pedigree Case-Control Studies Germ-Line Mutation Risk Factors Disease Susceptibility Genetic Testing Phenotype Haplotypes Mutation Genetic Markers Genetic Linkage Family Health Neoplastic Syndromes, Hereditary Gene-Environment Interaction Pelvimetry Chromosome Mapping Age of Onset Genetic Association Studies Genetic Variation DNA Mutational Analysis Disease Models, Animal Heredity Genome-Wide Association Study HLA-DQ Antigens Twins, Monozygotic Linkage Disequilibrium Heterozygote Family Obesity Hungary Penetrance Microsatellite Repeats Diabetes Mellitus, Type 2 HLA-DQ beta-Chains Genetic Loci Cohort Studies Time Factors Polymerase Chain Reaction Genes, BRCA1 Asian Continental Ancestry Group Age Factors Diseases in Twins European Continental Ancestry Group Incidence Homozygote Neoplasms Neoplasms, Multiple Primary Environment Base Sequence HLA-DRB1 Chains Causality Polymorphism, Single-Stranded Conformational Pregnancy Polymorphism, Restriction Fragment Length Odds Ratio Risk Autoimmune Diseases Prevalence Molecular Sequence Data Breast Neoplasms Risk Assessment Mice, Inbred Strains Infant, Newborn Inheritance Patterns Neoplasms, Second Primary Syndrome Autoantibodies Body Mass Index Models, Genetic Sex Factors Mice, Inbred C57BL Hypertension Autoimmunity Japan China Crosses, Genetic Chromosomes, Human, Pair 2 Smoking Thyroiditis, Autoimmune Lod Score Chromosomes, Human, Pair 6 HLA Antigens Liver Cirrhosis, Biliary Crohn Disease Species Specificity Diabetes Mellitus, Type 1 Celiac Disease Prospective Studies HLA-DR Antigens Diet Exons Chi-Square Distribution Chromosome Aberrations Promoter Regions, Genetic

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