Form of genetic mutations genetic predisposition to disease. Medical search. Frequent questions

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Anatomy9

Cell Line Brain Chromosomes, Human, Pair 2 Cells, Cultured Cell Line, Tumor Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 7 Mitochondria Neurons

Organisms9

Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Mice, Mutant Strains Mice, Inbred Strains Zebrafish Escherichia coli Caenorhabditis elegans Saccharomyces cerevisiae

Diseases44

Genetic Predisposition to Disease Disease Models, Animal Disease Susceptibility Syndrome Neoplastic Syndromes, Hereditary Neoplasms Fructose-1,6-Diphosphatase Deficiency Breast Neoplasms Obesity Diabetes Mellitus, Type 2 Disease Progression Cell Transformation, Neoplastic Deafness Diseases in Twins Neoplasms, Multiple Primary Autoimmune Diseases Skin Neoplasms Neoplasms, Second Primary Colorectal Neoplasms Hypertension Thyroiditis, Autoimmune Crohn Disease Liver Cirrhosis, Biliary Chromosome Aberrations Celiac Disease Parkinson Disease Li-Fraumeni Syndrome Diabetes Mellitus, Type 1 Lung Neoplasms Thyroid Neoplasms Diabetic Nephropathies Alcoholism Adenocarcinoma Adenomatous Polyposis Coli Colorectal Neoplasms, Hereditary Nonpolyposis Bloom Syndrome Leukemia, Myeloid, Acute Fanconi Anemia Lupus Erythematosus, Systemic Sjogren's Syndrome Colitis, Ulcerative Inflammation Inflammatory Bowel Diseases Body Weight

Chemicals and Drugs40

Genetic Markers Codon, Nonsense DNA-Binding Proteins DNA DNA Primers Carrier Proteins Nuclear Proteins HLA-DQ Antigens RNA, Messenger Transcription Factors Mutant Proteins Proto-Oncogene Proteins B-raf DNA, Neoplasm HLA-DQ beta-Chains Membrane Proteins Factor V Tumor Suppressor Proteins HLA-DRB1 Chains Tumor Suppressor Protein p53 Eye Proteins Proteins Neoplasm Proteins Codon HLA Antigens BRCA2 Protein Autoantibodies HLA-DR Antigens RecQ Helicases Nerve Tissue Proteins Prothrombin Peptidyl-Dipeptidase A BRCA1 Protein Carcinogens Bacterial Proteins DNA, Mitochondrial Proto-Oncogene Proteins MutS Homolog 2 Protein Protein-Serine-Threonine Kinases Mutagens Recombinant Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment44

Pedigree Genetic Testing DNA Mutational Analysis Polymerase Chain Reaction Case-Control Studies Risk Factors Sequence Analysis, DNA Chromosome Mapping Disease Models, Animal Amino Acid Substitution Genetic Association Studies Models, Genetic Pelvimetry Models, Biological Cohort Studies Genome-Wide Association Study Obesity Mutagenesis, Site-Directed Crosses, Genetic Gene Expression Profiling Transfection Risk Incidence Oligonucleotide Array Sequence Analysis Prognosis Models, Molecular Risk Assessment Odds Ratio Prevalence Reverse Transcriptase Polymerase Chain Reaction Immunohistochemistry Heterozygote Detection Body Mass Index Genetic Complementation Test Cloning, Molecular Sequence Alignment Retrospective Studies Chi-Square Distribution Blotting, Western Prospective Studies Mutagenesis, Insertional Logistic Models Reference Values Body Weight

Psychiatry and Psychology8

Family Siblings Smoking Schizophrenia Life Style Alcoholism Anxiety Motor Activity

Phenomena and Processes100

Genetic Predisposition to Disease Mutation Point Mutation Mutation, Missense Genotype Germ-Line Mutation Alleles Phenotype Polymorphism, Genetic Polymorphism, Single Nucleotide Heterozygote Frameshift Mutation Gene Frequency Exons Base Sequence Homozygote Polymorphism, Single-Stranded Conformational Genetic Linkage Genetic Markers Disease Susceptibility Genetic Variation Haplotypes Amino Acid Substitution Codon, Nonsense Genes, Recessive Mutation Rate Amino Acid Sequence Signal Transduction Penetrance Genes, BRCA1 Gene-Environment Interaction Promoter Regions, Genetic Genes, p53 Microsatellite Repeats Epigenesis, Genetic Heredity Time Factors Protein Structure, Tertiary Gene Deletion Genetic Loci Linkage Disequilibrium Obesity Mutagenesis Polymorphism, Restriction Fragment Length Species Specificity DNA Methylation Gene Expression Regulation Genes, Dominant Sequence Deletion Gene Expression Transfection Risk Protein Binding Inheritance Patterns Environment Lod Score Transcription, Genetic Chromosomes, Human, Pair 2 Pregnancy Aging Codon Gene Expression Regulation, Neoplastic Odds Ratio Chromosomes, Human, Pair 6 Suppression, Genetic Founder Effect Sequence Homology, Amino Acid Binding Sites Chromosomes, Human, Pair 7 Genome, Human Autoimmunity DNA Repair Drug Resistance Exome Genes, BRCA2 Body Mass Index Chromosome Aberrations Gene Silencing Consanguinity Chi-Square Distribution Gene Expression Regulation, Developmental Cell Proliferation Recombination, Genetic Apoptosis Genes, Lethal Plasmids Diet Quantitative Trait Loci Introns Mutagenesis, Insertional RNA Interference Protein Folding Genetic Heterogeneity Loss of Heterozygosity Genes, ras Genes Protein Conformation Body Weight Motor Activity Immunity, Innate

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena2

Family Siblings

Information Science5

Base Sequence Molecular Sequence Data Amino Acid Sequence Incidence Prevalence

Named Groups8

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

Health Care23

Genetic Testing Family Health Case-Control Studies Risk Factors Age of Onset Cohort Studies Genome-Wide Association Study Age Factors Genetic Counseling Risk Incidence Environment Causality Risk Assessment Odds Ratio Prevalence Body Mass Index Sex Factors Retrospective Studies Environmental Exposure Chi-Square Distribution Prospective Studies Logistic Models

Geographicals5

China Hungary Japan Germany France

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 Mutation Point Mutation Mutation, Missense Pedigree Genotype Germ-Line Mutation Alleles Genetic Testing Phenotype DNA Mutational Analysis Polymorphism, Genetic Polymorphism, Single Nucleotide Heterozygote Frameshift Mutation Gene Frequency Family Health Exons Base Sequence Polymerase Chain Reaction Case-Control Studies Homozygote Polymorphism, Single-Stranded Conformational Risk Factors Genetic Linkage Molecular Sequence Data Genetic Markers Sequence Analysis, DNA Chromosome Mapping Disease Models, Animal Age of Onset Disease Susceptibility Genetic Variation Haplotypes Amino Acid Substitution Codon, Nonsense Syndrome Neoplastic Syndromes, Hereditary Genes, Recessive Neoplasms Asian Continental Ancestry Group Mutation Rate Amino Acid Sequence Genetic Association Studies Models, Genetic DNA-Binding Proteins Signal Transduction Penetrance Genes, BRCA1 Gene-Environment Interaction DNA Promoter Regions, Genetic DNA Primers Genes, p53 Microsatellite Repeats Family Mice, Transgenic Fructose-1,6-Diphosphatase Deficiency Epigenesis, Genetic Pelvimetry Breast Neoplasms Models, Biological Mice, Inbred C57BL Cohort Studies Heredity Infant, Newborn Cell Line Genome-Wide Association Study Time Factors Protein Structure, Tertiary China Gene Deletion Genetic Loci Twins, Monozygotic Age Factors Brain Carrier Proteins Nuclear Proteins Mice, Knockout HLA-DQ Antigens Hungary Linkage Disequilibrium Obesity Diabetes Mellitus, Type 2 RNA, Messenger Transcription Factors Genetic Counseling Mutant Proteins Mutagenesis, Site-Directed Mutagenesis European Continental Ancestry Group Polymorphism, Restriction Fragment Length Proto-Oncogene Proteins B-raf Species Specificity Disease Progression DNA, Neoplasm DNA Methylation Cell Transformation, Neoplastic HLA-DQ beta-Chains Crosses, Genetic

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