Disease and treatment genetic predisposition to disease. Medical search. Frequent questions

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Anatomy6

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

Organisms6

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

Diseases56

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

Chemicals and Drugs38

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment41

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

Psychiatry and Psychology11

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

Phenomena and Processes72

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

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 Risk Environment Causality Age Factors Incidence Odds Ratio Risk Assessment Body Mass Index Prevalence Environmental Exposure Sex Factors Chi-Square Distribution Prospective Studies Logistic Models Analysis of Variance Questionnaires Regression Analysis Severity of Illness Index Retrospective Studies Registries Follow-Up Studies Longitudinal Studies Genetic Counseling

Geographicals7

Hungary China Japan Germany France Utah United States

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

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