Variants genetic predisposition to disease. Medical search. Frequent questions

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Anatomy9

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

Organisms5

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

Diseases56

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

Chemicals and Drugs39

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment48

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

Psychiatry and Psychology10

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

Phenomena and Processes84

Genetic Predisposition to Disease Genotype Polymorphism, Single Nucleotide Polymorphism, Genetic Alleles Gene Frequency Genetic Variation Germ-Line Mutation Phenotype Mutation Haplotypes Disease Susceptibility Genetic Markers Genetic Linkage Gene-Environment Interaction Heredity Base Sequence Genetic Loci Heterozygote Penetrance Obesity Homozygote Genes, BRCA1 Microsatellite Repeats Linkage Disequilibrium Exons Risk Polymorphism, Single-Stranded Conformational Environment Odds Ratio Inheritance Patterns Polymorphism, Restriction Fragment Length Genome, Human Pregnancy Promoter Regions, Genetic Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 2 Alternative Splicing Amino Acid Sequence Body Mass Index Lod Score Autoimmunity Time Factors Species Specificity Chromosomes, Human, Pair 7 Quantitative Trait Loci Chi-Square Distribution Diet Mutation, Missense Chromosome Aberrations Exome Signal Transduction Epigenesis, Genetic Body Weight Gene Expression Regulation Gene Expression Immunity, Innate Motor Activity Aging Amino Acid Substitution DNA Repair Homeostasis Blood Pressure Point Mutation Insulin Resistance Genes, BRCA2 Sequence Deletion Gene Deletion Protein Structure, Tertiary Genetic Heterogeneity Protein Binding DNA Damage Sequence Homology, Amino Acid Frameshift Mutation Genomic Instability Phylogeny Chromosomes, Human, Pair 9 Introns Recombination, Genetic Genes, Tumor Suppressor DNA Mismatch Repair DNA Copy Number Variations Binding Sites Genes, Dominant

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Family Siblings

Information Science8

Molecular Sequence Data Base Sequence Incidence Amino Acid Sequence Prevalence Questionnaires Registries Phylogeny

Named Groups9

European Continental Ancestry Group Twins, Monozygotic 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 Genome-Wide Association Study Age of Onset Cohort Studies Risk Environment Age Factors Incidence Odds Ratio Causality Risk Assessment Body Mass Index Prevalence Sex Factors Environmental Exposure Chi-Square Distribution Prospective Studies Logistic Models Analysis of Variance Regression Analysis Retrospective Studies Questionnaires Severity of Illness Index Follow-Up Studies Longitudinal Studies Registries Genetic Counseling

Geographicals7

Hungary China Japan Germany France United States Utah

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

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