Genetic disorders predictive value of tests. Medical search. Frequent questions

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Anatomy7

Brain Fibroblasts Chromosomes, Human, Pair 22 Cells, Cultured Cell Line Skin Chromosomes, Human, X

Organisms4

Mice, Knockout Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic

Diseases86

Genetic Diseases, Inborn Syndrome Williams Syndrome Bone Diseases, Developmental Musculoskeletal Abnormalities Metabolism, Inborn Errors Prader-Willi Syndrome Substance-Related Disorders Iron Metabolism Disorders Chromosome Disorders Ataxia Telangiectasia Neurofibromatosis 1 Genetic Predisposition to Disease Progeria Abnormalities, Multiple Pachyonychia Congenita Ectodermal Dysplasia Bloom Syndrome Disease Models, Animal Tuberous Sclerosis Rare Diseases Chondrodysplasia Punctata Myositis Ossificans Tic Disorders Fanconi Anemia Noonan Syndrome Skin Diseases, Genetic Nervous System Diseases Ossification, Heterotopic Cockayne Syndrome Hair Diseases Sleep Disorders 22q11 Deletion Syndrome Lymphoproliferative Disorders Intellectual Disability Kallmann Syndrome Lysosomal Storage Diseases Metal Metabolism, Inborn Errors Movement Disorders Turner Syndrome Marfan Syndrome Alcohol-Related Disorders Down Syndrome alpha 1-Antitrypsin Deficiency Chromosome Aberrations Osteogenesis Imperfecta Huntington Disease Cystic Fibrosis Myotonic Dystrophy Microcephaly Hemochromatosis beta-Thalassemia Lipid Metabolism, Inborn Errors Speech Disorders Hepatolenticular Degeneration Muscular Dystrophies Acrodermatitis Hydranencephaly Menkes Kinky Hair Syndrome Werner Syndrome Hypohidrosis Bardet-Biedl Syndrome Craniofacial Abnormalities Dysautonomia, Familial Xeroderma Pigmentosum Facies Rett Syndrome Rothmund-Thomson Syndrome Myeloproliferative Disorders Angelman Syndrome Sex Chromosome Aberrations Albinism, Oculocutaneous Dwarfism Immunologic Deficiency Syndromes Fragile X Syndrome Keratoderma, Palmoplantar Temporomandibular Joint Disorders Neurofibromatoses Recurrence Epidermolysis Bullosa Simplex Hemoglobinopathies Learning Disorders Hermanski-Pudlak Syndrome Disease Progression Alcoholism Acute Disease

Chemicals and Drugs24

Neurofibromin 1 Biological Markers RecQ Helicases Reagent Kits, Diagnostic Codon, Nonsense Reagent Strips DNA Helicases Proteins Radiopharmaceuticals RNA, Messenger Genetic Markers DNA Primers Fanconi Anemia Complementation Group G Protein Lamin Type A Tumor Markers, Biological Fluorodeoxyglucose F18 Membrane Proteins Fanconi Anemia Complementation Group Proteins TRPP Cation Channels DNA Tumor Suppressor Proteins Ataxia Telangiectasia Mutated Proteins Nuclear Proteins DNA-Binding Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment60

Predictive Value of Tests Sensitivity and Specificity ROC Curve Prospective Studies Reproducibility of Results Pedigree Retrospective Studies Risk Factors Genetic Testing Prognosis False Positive Reactions Severity of Illness Index Prenatal Diagnosis False Negative Reactions Treatment Outcome Polymerase Chain Reaction Follow-Up Studies Cohort Studies Case-Control Studies Prevalence Magnetic Resonance Imaging Tomography, X-Ray Computed Disease Models, Animal DNA Mutational Analysis Mass Screening Reagent Kits, Diagnostic Risk Assessment Questionnaires Evaluation Studies as Topic Reagent Strips Heterozygote Detection Preimplantation Diagnosis Chromosome Mapping Biopsy Cross-Sectional Studies Logistic Models Genetic Therapy Reference Values Bacteriological Techniques Models, Biological Diagnostic Errors Positron-Emission Tomography Incidence Enzyme-Linked Immunosorbent Assay Multivariate Analysis Early Diagnosis Immunohistochemistry Observer Variation Sequence Analysis, DNA Facies Longitudinal Studies Analysis of Variance Models, Genetic Chi-Square Distribution Ultrasonography, Doppler, Color Epidemiologic Methods Regression Analysis Electrocardiography Biopsy, Fine-Needle Area Under Curve

Psychiatry and Psychology39

Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Depressive Disorder, Major Autistic Disorder Attention Deficit Disorder with Hyperactivity Depressive Disorder Stress Disorders, Post-Traumatic Obsessive-Compulsive Disorder Psychotic Disorders Substance-Related Disorders Phobic Disorders Child Development Disorders, Pervasive Psychiatric Status Rating Scales Conduct Disorder Tic Disorders Cognition Disorders Borderline Personality Disorder Somatoform Disorders Sleep Disorders Intellectual Disability Alcohol-Related Disorders Huntington Disease Developmental Disabilities Combat Disorders Attention Deficit and Disruptive Behavior Disorders Schizophrenia Impulse Control Disorders Neuropsychological Tests Interview, Psychological Antisocial Personality Disorder Binge-Eating Disorder Dysthymic Disorder Dissociative Disorders Conversion Disorder Learning Disorders Alcoholism Schizotypal Personality Disorder

Phenomena and Processes37

Sensitivity and Specificity Mutation Phenotype Genes, Recessive Pregnancy Time Factors Heterozygote Genetic Predisposition to Disease Consanguinity Genotype Alleles Base Sequence Mutation, Missense Point Mutation Codon, Nonsense Genetic Linkage Genes, Neurofibromatosis 1 Exons Homozygote Endophenotypes Algorithms Amino Acid Sequence Chromosome Aberrations Genes, Dominant Polymorphism, Single Nucleotide Chromosomes, Human, Pair 22 Genetic Markers Frameshift Mutation Exome Haplotypes Signal Transduction Sex Chromosome Aberrations Genome, Human Chi-Square Distribution Polymorphism, Genetic Chromosomes, Human, X Area Under Curve

Disciplines and Occupations4

Genetic Counseling Genetics, Medical Immunohistochemistry Genetic Research

Humanities1

Information Science9

Diagnostic and Statistical Manual of Mental Disorders Molecular Sequence Data Prevalence Base Sequence Questionnaires Algorithms Amino Acid Sequence International Classification of Diseases Incidence

Named Groups1

Infant, Newborn

Health Care37

Predictive Value of Tests Sensitivity and Specificity ROC Curve Prospective Studies Reproducibility of Results Retrospective Studies Risk Factors Genetic Testing Genetic Counseling Severity of Illness Index Genetic Services Treatment Outcome Follow-Up Studies Cohort Studies Case-Control Studies Prevalence Mass Screening Comorbidity Risk Assessment Questionnaires Evaluation Studies as Topic Age Factors Cross-Sectional Studies Logistic Models Age of Onset Diagnostic Errors Incidence Multivariate Analysis Family Health Observer Variation Longitudinal Studies Analysis of Variance Chi-Square Distribution Epidemiologic Methods Regression Analysis Sex Factors Area Under Curve

Geographicals2

Mediterranean Islands United States

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

Predictive Value of Tests Genetic Diseases, Inborn Sensitivity and Specificity Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Mutation Diagnostic and Statistical Manual of Mental Disorders ROC Curve Prospective Studies Reproducibility of Results Syndrome Depressive Disorder, Major Phenotype Williams Syndrome Pedigree Autistic Disorder Bone Diseases, Developmental Musculoskeletal Abnormalities Attention Deficit Disorder with Hyperactivity Retrospective Studies Depressive Disorder Metabolism, Inborn Errors Risk Factors Genetic Testing Stress Disorders, Post-Traumatic Obsessive-Compulsive Disorder Prognosis False Positive Reactions Genes, Recessive Genetic Counseling Prader-Willi Syndrome Severity of Illness Index Psychotic Disorders Pregnancy Substance-Related Disorders Phobic Disorders Time Factors Infant, Newborn Child Development Disorders, Pervasive Iron Metabolism Disorders Prenatal Diagnosis False Negative Reactions Chromosome Disorders Genetic Services Mediterranean Islands Treatment Outcome Ataxia Telangiectasia Heterozygote Neurofibromin 1 Neurofibromatosis 1 Molecular Sequence Data Polymerase Chain Reaction Follow-Up Studies Genetic Predisposition to Disease Progeria Cohort Studies Eugenics Case-Control Studies Prevalence Magnetic Resonance Imaging Biological Markers Tomography, X-Ray Computed Abnormalities, Multiple Pachyonychia Congenita Ectodermal Dysplasia Bloom Syndrome Disease Models, Animal Tuberous Sclerosis Psychiatric Status Rating Scales Conduct Disorder Rare Diseases Consanguinity Genotype DNA Mutational Analysis Chondrodysplasia Punctata Myositis Ossificans Tic Disorders Alleles Brain Fanconi Anemia Base Sequence Noonan Syndrome Skin Diseases, Genetic Nervous System Diseases Mass Screening Mutation, Missense Ossification, Heterotopic Cognition Disorders RecQ Helicases Reagent Kits, Diagnostic Cockayne Syndrome Comorbidity Risk Assessment Questionnaires Point Mutation Borderline Personality Disorder Genetics, Medical Somatoform Disorders

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