Predispositions 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 Chromosomes, Human, Pair 11

Organisms7

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

Diseases60

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

Chemicals and Drugs41

Genetic Markers HLA-DQ Antigens HLA-DQ beta-Chains RecQ Helicases HLA-DRB1 Chains HLA-DR Antigens HLA Antigens DNA-Binding Proteins Autoantibodies BRCA2 Protein Peptidyl-Dipeptidase A DNA Proteins BRCA1 Protein Fanconi Anemia Complementation Group Proteins Tumor Suppressor Proteins DNA Helicases MutS Homolog 2 Protein Carrier Proteins Carcinogens Ataxia Telangiectasia Mutated Proteins Ethanol Biological Markers HLA-DR Serological Subtypes RNA, Messenger Fanconi Anemia Complementation Group C Protein Nuclear Proteins DNA, Neoplasm Cytokines Protein-Serine-Threonine Kinases Cell Cycle Proteins Tumor Necrosis Factor-alpha Fanconi Anemia Complementation Group E Protein Fanconi Anemia Complementation Group G Protein DNA Repair Enzymes Insulin Neoplasm Proteins Blood Glucose Fanconi Anemia Complementation Group D2 Protein Neurofibromin 1 HLA-B51 Antigen

Analytical, Diagnostic and Therapeutic Techniques and Equipment43

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

Psychiatry and Psychology11

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

Phenomena and Processes79

Genetic Predisposition to Disease Genotype Polymorphism, Genetic Alleles Germ-Line Mutation Polymorphism, Single Nucleotide Disease Susceptibility Gene Frequency Phenotype Haplotypes Mutation Genetic Markers Genetic Linkage Gene-Environment Interaction Penetrance Heredity Genes, BRCA1 Heterozygote Genetic Variation Obesity Linkage Disequilibrium Genetic Loci Microsatellite Repeats Homozygote Risk Polymorphism, Single-Stranded Conformational Environment Lod Score Odds Ratio Base Sequence Pregnancy Polymorphism, Restriction Fragment Length Autoimmunity Inheritance Patterns Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Body Mass Index Exons Time Factors Chromosomes, Human, Pair 7 Promoter Regions, Genetic Genome, Human Chromosome Aberrations DNA Repair Chi-Square Distribution Species Specificity Diet Quantitative Trait Loci Genes, BRCA2 Epigenesis, Genetic Body Weight Aging Signal Transduction Immunity, Innate Motor Activity Mutation, Missense Genomic Instability Blood Pressure DNA Damage Homeostasis Gene Expression Regulation Genes, Tumor Suppressor Loss of Heterozygosity DNA Mismatch Repair Gene Expression Insulin Resistance Exome Gene Deletion Genes, p16 Genes, APC Genetic Heterogeneity Base Pair Mismatch Genes, p53 Point Mutation Chromosomes, Human, Pair 9 Frameshift Mutation Chromosomes, Human, Pair 11 Haploinsufficiency Sex Characteristics

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena3

Family Siblings Dermatoglyphics

Humanities1

Church of Jesus Christ of Latter-day Saints

Information Science6

Incidence Base Sequence Molecular Sequence Data Prevalence Questionnaires Registries

Named Groups9

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

Health Care30

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

Geographicals8

Hungary Utah China Japan Germany France United States Finland

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

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

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