Onset genetic predisposition to disease. Medical search. Frequent questions

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Anatomy8

Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 7 Brain Adipose Tissue Intestinal Mucosa Chromosomes, Human, Pair 9 Cells, Cultured

Organisms7

Mice, Inbred Strains Mice, Inbred C57BL Mice, Transgenic Mice, Knockout Mice, Inbred BALB C Rats, Inbred BB Chrysanthemum

Diseases57

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

Chemicals and Drugs40

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

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

Psychiatry and Psychology11

Family Schizophrenia Smoking Siblings Alcoholism Life Style Stress, Psychological Anxiety Motor Activity Alcohol Drinking Imprinting (Psychology)

Phenomena and Processes80

Genetic Predisposition to Disease Genotype Polymorphism, Genetic Alleles Polymorphism, Single Nucleotide Germ-Line Mutation Gene Frequency Disease Susceptibility Phenotype Haplotypes Genetic Markers Mutation Genetic Linkage Gene-Environment Interaction Heredity Obesity Penetrance Genetic Variation Genetic Loci Linkage Disequilibrium Heterozygote Genes, BRCA1 Microsatellite Repeats Time Factors Risk Environment Homozygote Pregnancy Polymorphism, Single-Stranded Conformational Odds Ratio Autoimmunity Inheritance Patterns Lod Score Chromosomes, Human, Pair 2 Body Mass Index Chromosomes, Human, Pair 6 Base Sequence Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 7 Promoter Regions, Genetic Chi-Square Distribution Exons Diet Species Specificity Genome, Human Quantitative Trait Loci Chromosome Aberrations Body Weight Motor Activity Epigenesis, Genetic Immunity, Innate Aging Signal Transduction Homeostasis Gene Expression Regulation DNA Repair Blood Pressure Gene Expression Insulin Resistance Genes, BRCA2 Mutation, Missense Labor Onset DNA Damage Genomic Instability Gene Deletion Genes, Tumor Suppressor Loss of Heterozygosity DNA Mismatch Repair Genetic Heterogeneity Exome Point Mutation Sex Characteristics Genes, Dominant Genes, APC Base Pair Mismatch Genes, p53 Genes, p16 Chromosomes, Human, Pair 9 Frameshift Mutation Genes, Recessive

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Family Siblings

Humanities1

Church of Jesus Christ of Latter-day Saints

Information Science6

Incidence Prevalence Base Sequence Molecular Sequence Data Questionnaires Registries

Named Groups9

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

Health Care30

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

Geographicals8

Hungary Japan China Germany France United States Utah Finland

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 Genotype Polymorphism, Genetic Alleles Polymorphism, Single Nucleotide Pedigree Germ-Line Mutation Gene Frequency Case-Control Studies Risk Factors Disease Susceptibility Genetic Testing Phenotype Haplotypes Family Health Genetic Markers Mutation Genetic Linkage Neoplastic Syndromes, Hereditary Gene-Environment Interaction Pelvimetry Disease Models, Animal Age of Onset Genetic Association Studies Chromosome Mapping Heredity Genome-Wide Association Study HLA-DQ Antigens Twins, Monozygotic DNA Mutational Analysis Family Obesity Penetrance Diabetes Mellitus, Type 2 Hungary HLA-DQ beta-Chains Genetic Variation Genetic Loci Linkage Disequilibrium Heterozygote European Continental Ancestry Group Genes, BRCA1 Cohort Studies Diseases in Twins Microsatellite Repeats Age Factors Time Factors HLA-DRB1 Chains Neoplasms, Multiple Primary Incidence Risk Environment Neoplasms Causality Asian Continental Ancestry Group Homozygote Autoimmune Diseases Pregnancy Polymerase Chain Reaction Polymorphism, Single-Stranded Conformational Odds Ratio Syndrome Neoplasms, Second Primary Breast Neoplasms Risk Assessment Mice, Inbred Strains Autoantibodies HLA Antigens Autoimmunity Inheritance Patterns Lod Score Diabetes Mellitus, Type 1 Thyroiditis, Autoimmune Hypertension Chromosomes, Human, Pair 2 HLA-DR Antigens Infant, Newborn Prevalence Body Mass Index Liver Cirrhosis, Biliary Chromosomes, Human, Pair 6 Base Sequence Crohn Disease Celiac Disease Schizophrenia Mice, Inbred C57BL Sex Factors Smoking Disease Progression Polymorphism, Restriction Fragment Length Siblings Molecular Sequence Data Diabetic Nephropathies Chromosomes, Human, Pair 7 Japan Twins, Dizygotic Skin Neoplasms Crosses, Genetic Environmental Exposure China

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