Estimate the penetrance. Medical search. Frequent questions

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Anatomy1

Chromosomes, Human, Pair 19

Organisms2

Mice, Transgenic Mice, Inbred C57BL

Diseases25

Genetic Predisposition to Disease Optic Atrophy, Hereditary, Leber Hirschsprung Disease Genetic Diseases, Inborn Syndrome Dystonia Musculorum Deformans Dystonia Amyloid Neuropathies, Familial Breast Neoplasms Hemochromatosis Angiomatosis Abnormalities, Multiple Syndactyly Craniofacial Abnormalities Retinoblastoma Neoplastic Syndromes, Hereditary Cardiomyopathy, Hypertrophic, Familial Ovarian Neoplasms Myoclonus Retinitis Pigmentosa Optic Atrophies, Hereditary Disease Models, Animal Dystonic Disorders Paraganglioma, Extra-Adrenal Eye Abnormalities

Chemicals and Drugs8

Genetic Markers BRCA2 Protein DNA, Mitochondrial Proto-Oncogene Proteins c-ret Prealbumin RNA, Transfer, Ile Bone Morphogenetic Protein Receptors, Type II Transcription Factors

Analytical, Diagnostic and Therapeutic Techniques and Equipment28

Pedigree Models, Genetic Genetic Testing DNA Mutational Analysis Chromosome Mapping Likelihood Functions Models, Statistical Risk Factors Crosses, Genetic Heterozygote Detection Prevalence Reproducibility of Results Case-Control Studies Probability Cohort Studies Incidence Risk Assessment Risk Models, Biological Data Interpretation, Statistical Sequence Analysis, DNA Bayes Theorem Breeding Genetic Association Studies Models, Theoretical Disease Models, Animal Polymerase Chain Reaction Sensitivity and Specificity

Psychiatry and Psychology2

Family Nuclear Family

Phenomena and Processes39

Penetrance Genes, Dominant Heterozygote Phenotype Mutation Genetic Linkage Genetic Predisposition to Disease Alleles Lod Score Genotype Germ-Line Mutation Genes, BRCA1 Haplotypes Founder Effect Genes, Modifier Gene Frequency Genetic Variation Homozygote Genetic Heterogeneity Genes, Recessive Genetic Markers Genes, BRCA2 Mutation, Missense Polymorphism, Single Nucleotide Algorithms Probability Inheritance Patterns Microsatellite Repeats Time Factors Risk Epistasis, Genetic Chromosomes, Human, Pair 19 Breeding Exons Base Sequence Point Mutation Linkage Disequilibrium Sensitivity and Specificity Environment

Disciplines and Occupations3

Genetic Counseling Genetics, Medical Genetics, Population

Anthropology, Education, Sociology and Social Phenomena2

Family Nuclear Family

Information Science7

Computer Simulation Prevalence Algorithms Incidence Data Interpretation, Statistical Molecular Sequence Data Base Sequence

Named Groups2

Jews Infant, Newborn

Health Care21

Family Health Genetic Testing Age of Onset Likelihood Functions Models, Statistical Risk Factors Prevalence Reproducibility of Results Case-Control Studies Genetic Counseling Probability Cohort Studies Age Factors Incidence Risk Assessment Risk Data Interpretation, Statistical Bayes Theorem Sex Factors Sensitivity and Specificity Environment

Geographicals1

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

Penetrance Pedigree Genes, Dominant Heterozygote Phenotype Mutation Genetic Linkage Genetic Predisposition to Disease Models, Genetic Alleles Lod Score Genotype Optic Atrophy, Hereditary, Leber Family Health Germ-Line Mutation Genetic Testing DNA Mutational Analysis Genes, BRCA1 Chromosome Mapping Age of Onset Haplotypes Founder Effect Genes, Modifier Likelihood Functions Models, Statistical Gene Frequency Hirschsprung Disease Genetic Variation Homozygote Jews Genetic Heterogeneity Genes, Recessive Genetic Markers Genetic Diseases, Inborn Family Risk Factors Crosses, Genetic Computer Simulation Genes, BRCA2 Mutation, Missense Syndrome Dystonia Musculorum Deformans Heterozygote Detection Prevalence Reproducibility of Results BRCA2 Protein Polymorphism, Single Nucleotide Algorithms Case-Control Studies Dystonia Genetic Counseling United States Probability Amyloid Neuropathies, Familial DNA, Mitochondrial Breast Neoplasms Cohort Studies Age Factors Inheritance Patterns Microsatellite Repeats Time Factors Incidence Risk Assessment Risk Epistasis, Genetic Hemochromatosis Models, Biological Genetics, Medical Angiomatosis Data Interpretation, Statistical Abnormalities, Multiple Molecular Sequence Data Syndactyly Sequence Analysis, DNA Proto-Oncogene Proteins c-ret Craniofacial Abnormalities Retinoblastoma Chromosomes, Human, Pair 19 Bayes Theorem Prealbumin Sex Factors Breeding RNA, Transfer, Ile Neoplastic Syndromes, Hereditary Cardiomyopathy, Hypertrophic, Familial Genetic Association Studies Bone Morphogenetic Protein Receptors, Type II Exons Ovarian Neoplasms Genetics, Population Myoclonus Models, Theoretical Mice, Transgenic Base Sequence Mice, Inbred C57BL Point Mutation Infant, Newborn Retinitis Pigmentosa Optic Atrophies, Hereditary Disease Models, Animal

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