Predisposition gene. Medical search. Frequent questions

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Anatomy3

Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 6

Organisms4

Mice, Inbred C57BL Mice, Knockout Chrysanthemum Rats, Inbred BB

Diseases40

Genetic Predisposition to Disease Breast Neoplasms Disease Susceptibility Neoplastic Syndromes, Hereditary Bloom Syndrome Fanconi Anemia Li-Fraumeni Syndrome Ataxia Telangiectasia Rothmund-Thomson Syndrome Adenomatous Polyposis Coli Neoplasms Colorectal Neoplasms, Hereditary Nonpolyposis Syndrome Peutz-Jeghers Syndrome Nijmegen Breakage Syndrome Disease Models, Animal Neurofibromatoses Werner Syndrome Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome Neurofibromatosis 1 Hereditary Breast and Ovarian Cancer Syndrome Genomic Instability Retinoblastoma Neoplasms, Multiple Primary Wilms Tumor Obesity Skin Neoplasms Chromosome Aberrations Colorectal Neoplasms Ovarian Neoplasms Costello Syndrome Autoimmune Diseases Diabetes Mellitus, Type 2 Dog Diseases Diabetes Mellitus, Type 1 von Hippel-Lindau Disease Hamartoma Syndrome, Multiple Diseases in Twins Multiple Endocrine Neoplasia

Chemicals and Drugs29

BRCA2 Protein RecQ Helicases Genetic Markers BRCA1 Protein DNA-Binding Proteins HLA-DQ Antigens 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 HLA-DRB1 Chains Cell Cycle Proteins HLA-DR Antigens Fanconi Anemia Complementation Group E Protein HLA-DQ beta-Chains Fanconi Anemia Complementation Group G Protein DNA Repair Enzymes Neoplasm Proteins DNA Proteins Fanconi Anemia Complementation Group D2 Protein Neurofibromin 1 HLA-B51 Antigen

Analytical, Diagnostic and Therapeutic Techniques and Equipment20

Pedigree Genetic Testing Case-Control Studies Risk Factors DNA Mutational Analysis Chromosome Mapping Disease Models, Animal Polymerase Chain Reaction Genome-Wide Association Study Genetic Association Studies Cohort Studies Obesity Risk Models, Genetic Odds Ratio Heterozygote Detection Risk Assessment Incidence Dermatoglyphics Sequence Analysis, DNA

Psychiatry and Psychology3

Family Imprinting (Psychology)Siblings

Phenomena and Processes58

Genetic Predisposition to Disease Germ-Line Mutation Genetic Linkage Genes, BRCA1 Mutation Disease Susceptibility Alleles Genotype Polymorphism, Genetic Polymorphism, Single Nucleotide Gene Frequency Phenotype Haplotypes Penetrance Heterozygote Genetic Markers DNA Repair Genetic Variation Genes, BRCA2 Linkage Disequilibrium Microsatellite Repeats Base Sequence Homozygote Lod Score Heredity Polymorphism, Single-Stranded Conformational Mutation, Missense Genomic Instability Exons DNA Damage Genetic Loci Polymorphism, Restriction Fragment Length Obesity Gene-Environment Interaction Genes, Tumor Suppressor Loss of Heterozygosity Risk DNA Mismatch Repair Chromosome Aberrations Pregnancy Exome Gene Deletion Odds Ratio Genes, p16 Genes, APC Genetic Heterogeneity Base Pair Mismatch Environment Genes, p53 Point Mutation Chromosomes, Human, Pair 9 Genome, Human Frameshift Mutation Chromosomes, Human, Pair 11 Haploinsufficiency Sex Characteristics Time Factors Chromosomes, Human, Pair 6

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena3

Family Siblings Dermatoglyphics

Humanities1

Church of Jesus Christ of Latter-day Saints

Information Science3

Base Sequence Molecular Sequence Data Incidence

Named Groups6

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

Health Care16

Genetic Testing Case-Control Studies Risk Factors Family Health Age of Onset Genome-Wide Association Study Causality Age Factors Genetic Counseling Cohort Studies Sex Factors Risk Odds Ratio Environment Risk Assessment Incidence

Geographicals2

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 Humanities Information Science Named Groups Health Care Geographicals

Genetic Predisposition to Disease Pedigree Germ-Line Mutation BRCA2 Protein Genetic Linkage Genes, BRCA1 Breast Neoplasms Mutation Disease Susceptibility Alleles Genotype Neoplastic Syndromes, Hereditary Polymorphism, Genetic Polymorphism, Single Nucleotide Genetic Testing RecQ Helicases Gene Frequency Case-Control Studies Phenotype Bloom Syndrome Risk Factors Haplotypes Fanconi Anemia Li-Fraumeni Syndrome Family Health Utah DNA Mutational Analysis Penetrance Heterozygote Genetic Markers Ataxia Telangiectasia Chromosome Mapping DNA Repair Rothmund-Thomson Syndrome Adenomatous Polyposis Coli Neoplasms Colorectal Neoplasms, Hereditary Nonpolyposis Syndrome Genetic Variation Peutz-Jeghers Syndrome Family Age of Onset BRCA1 Protein Genes, BRCA2 DNA-Binding Proteins Nijmegen Breakage Syndrome Linkage Disequilibrium HLA-DQ Antigens Fanconi Anemia Complementation Group Proteins Tumor Suppressor Proteins Microsatellite Repeats Disease Models, Animal Base Sequence Neurofibromatoses Werner Syndrome Polymerase Chain Reaction Homozygote Lod Score Molecular Sequence Data Basal Cell Nevus Syndrome Heredity DNA Helicases MutS Homolog 2 Protein Genome-Wide Association Study Ataxia Telangiectasia Mutated Proteins Polymorphism, Single-Stranded Conformational Beckwith-Wiedemann Syndrome HLA-DR Serological Subtypes Neurofibromatosis 1 Hereditary Breast and Ovarian Cancer Syndrome Causality Mutation, Missense Genomic Instability Retinoblastoma Exons Neoplasms, Multiple Primary Jews Age Factors DNA Damage Genetic Association Studies Genetic Loci Fanconi Anemia Complementation Group C Protein Wilms Tumor Polymorphism, Restriction Fragment Length Mice, Inbred C57BL Genetic Counseling Cohort Studies Nuclear Proteins Obesity European Continental Ancestry Group DNA, Neoplasm Protein-Serine-Threonine Kinases Gene-Environment Interaction Genes, Tumor Suppressor HLA-DRB1 Chains Cell Cycle Proteins Asian Continental Ancestry Group Loss of Heterozygosity Sex Factors Risk

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