Hereditary cancer predisposition syndromes. Medical search. Frequent questions

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Anatomy5

Cell Line, Tumor Fibroblasts Cell Line HeLa Cells Cells, Cultured

Organisms3

Mice, Nude Mice, Knockout Mice, Mutant Strains

Diseases64

Neoplastic Syndromes, Hereditary Li-Fraumeni Syndrome Peutz-Jeghers Syndrome Colorectal Neoplasms, Hereditary Nonpolyposis Genetic Predisposition to Disease Adenomatous Polyposis Coli Neurofibromatosis 1 Rhabdoid Tumor Syndrome Optic Nerve Glioma Neurofibromatosis 2 Neoplasms von Hippel-Lindau Disease Breast Neoplasms Ovarian Neoplasms Bloom Syndrome Fanconi Anemia Werner Syndrome Rothmund-Thomson Syndrome Ataxia Telangiectasia Hereditary Breast and Ovarian Cancer Syndrome Metabolic Syndrome X Down Syndrome Neurofibromatoses Prostatic Neoplasms Disease Susceptibility Genomic Instability Colorectal Neoplasms Cockayne Syndrome Sjogren's Syndrome Nephrotic Syndrome Lung Neoplasms Colonic Neoplasms Stomach Neoplasms Cell Transformation, Neoplastic Neoplasm Metastasis Chromosome Aberrations Pancreatic Neoplasms Neoplasm Invasiveness Xeroderma Pigmentosum Turner Syndrome Disease Progression Myelodysplastic Syndromes Abnormalities, Multiple Cushing Syndrome Carcinoma Disease Models, Animal Uterine Cervical Neoplasms Carcinoma, Squamous Cell Polycystic Ovary Syndrome Urinary Bladder Neoplasms Acute Coronary Syndrome Williams Syndrome Long QT Syndrome Carcinoma, Non-Small-Cell Lung Hemolytic-Uremic Syndrome DiGeorge Syndrome Horner Syndrome Skin Neoplasms Prader-Willi Syndrome Endometrial Neoplasms Neoplasms, Multiple Primary Guillain-Barre Syndrome Rectal Neoplasms

Chemicals and Drugs39

Neurofibromin 1 MutS Homolog 2 Protein RecQ Helicases Von Hippel-Lindau Tumor Suppressor Protein BRCA2 Protein Fanconi Anemia Complementation Group E Protein DNA Helicases BRCA1 Protein Fanconi Anemia Complementation Group Proteins Ataxia Telangiectasia Mutated Proteins Tumor Suppressor Proteins DNA-Binding Proteins Fanconi Anemia Complementation Group D2 Protein Nuclear Proteins Cell Cycle Proteins Neoplasm Proteins Fanconi Anemia Complementation Group F Protein Fanconi Anemia Complementation Group L Protein DNA, Neoplasm Exodeoxyribonucleases Protein-Serine-Threonine Kinases Fanconi Anemia Complementation Group G Protein DNA Repair Enzymes Tumor Suppressor Protein p53 PTEN Phosphohydrolase DNA Adenosine Triphosphatases Rad51 Recombinase Cancer Vaccines Proteins Transcription Factors RNA, Messenger Adaptor Proteins, Signal Transducing Antineoplastic Agents Tumor Markers, Biological Genetic Markers Receptors, Estrogen RNA, Small Interfering Receptor, erbB-2

Analytical, Diagnostic and Therapeutic Techniques and Equipment38

Genetic Testing Pedigree DNA Mutational Analysis Early Detection of Cancer Risk Factors Case-Control Studies Polymerase Chain Reaction Chromosome Mapping Retrospective Studies Follow-Up Studies Prospective Studies Prognosis Risk Models, Biological Risk Assessment Reverse Transcriptase Polymerase Chain Reaction Survival Analysis Models, Genetic Survival Rate Gene Expression Profiling Odds Ratio Disease Models, Animal Registries Antineoplastic Combined Chemotherapy Protocols Treatment Outcome Blotting, Western Incidence Sensitivity and Specificity Neoplasm Staging Questionnaires Oligonucleotide Array Sequence Analysis Xenograft Model Antitumor Assays Cohort Studies Logistic Models Combined Modality Therapy Multivariate Analysis Predictive Value of Tests Prevalence

Psychiatry and Psychology1

Phenomena and Processes52

Germ-Line Mutation Genetic Predisposition to Disease Mutation Genes, BRCA1 Genes, BRCA2 DNA Repair Genotype Alleles Phenotype Penetrance DNA Damage Disease Susceptibility Genomic Instability DNA Mismatch Repair Polymorphism, Genetic Heterozygote Polymorphism, Single Nucleotide Mutation, Missense Base Sequence Base Pair Mismatch Radiation Tolerance Genes, Tumor Suppressor Exons Haplotypes Genes, APC Microsatellite Repeats Genes, p53 Homozygote Genetic Variation DNA Breaks, Double-Stranded Chromosome Aberrations Recombination, Genetic Gene Expression Regulation, Neoplastic Loss of Heterozygosity Cell Cycle Risk DNA Replication Signal Transduction Sequence Deletion Apoptosis Odds Ratio Point Mutation Gene Frequency Amino Acid Sequence DNA Methylation Phosphorylation Drug Resistance, Neoplasm Genetic Markers Sensitivity and Specificity Genetic Linkage Promoter Regions, Genetic Time Factors

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

National Cancer Institute (U.S.)

Information Science8

Base Sequence Molecular Sequence Data Survival Rate Registries Amino Acid Sequence Incidence Questionnaires Prevalence

Named Groups2

Survivors Infant, Newborn

Health Care26

Genetic Counseling Genetic Testing Risk Factors Case-Control Studies Family Health Retrospective Studies Follow-Up Studies Prospective Studies Risk Age Factors Risk Assessment Survival Analysis Survival Rate Odds Ratio Registries Treatment Outcome National Cancer Institute (U.S.)Incidence Sensitivity and Specificity Questionnaires Cohort Studies Logistic Models Age of Onset Multivariate Analysis Predictive Value of Tests Prevalence

Geographicals3

Finland United States China

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

Neoplastic Syndromes, Hereditary Li-Fraumeni Syndrome Peutz-Jeghers Syndrome Germ-Line Mutation Colorectal Neoplasms, Hereditary Nonpolyposis Genetic Predisposition to Disease Adenomatous Polyposis Coli Mutation Genetic Counseling Neurofibromatosis 1 Genetic Testing Neurofibromin 1 Rhabdoid Tumor Syndrome Genes, BRCA1 Pedigree Optic Nerve Glioma Neurofibromatosis 2 Genes, BRCA2 Neoplasms von Hippel-Lindau Disease MutS Homolog 2 Protein Breast Neoplasms Ovarian Neoplasms RecQ Helicases Bloom Syndrome Von Hippel-Lindau Tumor Suppressor Protein Fanconi Anemia Werner Syndrome Rothmund-Thomson Syndrome DNA Repair Ataxia Telangiectasia BRCA2 Protein Fanconi Anemia Complementation Group E Protein Genotype Alleles DNA Helicases BRCA1 Protein Hereditary Breast and Ovarian Cancer Syndrome Metabolic Syndrome X Phenotype Fanconi Anemia Complementation Group Proteins Penetrance Down Syndrome Ataxia Telangiectasia Mutated Proteins Tumor Suppressor Proteins DNA-Binding Proteins DNA Mutational Analysis Early Detection of Cancer DNA Damage Neurofibromatoses Prostatic Neoplasms Fanconi Anemia Complementation Group D2 Protein Disease Susceptibility Risk Factors Genomic Instability DNA Mismatch Repair Nuclear Proteins Cell Cycle Proteins Neoplasm Proteins Polymorphism, Genetic Fanconi Anemia Complementation Group F Protein Heterozygote Fanconi Anemia Complementation Group L Protein Colorectal Neoplasms DNA, Neoplasm Exodeoxyribonucleases Polymorphism, Single Nucleotide Protein-Serine-Threonine Kinases Case-Control Studies Cockayne Syndrome Family Health Fanconi Anemia Complementation Group G Protein Mutation, Missense DNA Repair Enzymes Base Sequence Sjogren's Syndrome Nephrotic Syndrome Lung Neoplasms Molecular Sequence Data Base Pair Mismatch Polymerase Chain Reaction Colonic Neoplasms Radiation Tolerance Stomach Neoplasms Tumor Suppressor Protein p53 Genes, Tumor Suppressor Exons Haplotypes Genes, APC Microsatellite Repeats Cell Transformation, Neoplastic Genes, p53 Homozygote Genetic Variation DNA Breaks, Double-Stranded Neoplasm Metastasis Cell Line, Tumor Chromosome Mapping Chromosome Aberrations

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