Mutations polycystic kidney autosomal dominant. Medical search. Frequent questions

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Anatomy26

Kidney Cilia Kidney Tubules Chromosomes, Human, Pair 16 Cyst Fluid Cell Line Kidney Cortex Kidney Tubules, Collecting Epithelial Cells Kidney Tubules, Proximal Cells, Cultured Kidney Glomerulus Nephrons Chromosomes, Human, Pair 4 Ovary Liver Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 6 Epithelium Kidney Medulla Chromosomes, Human, Pair 1 Cell Membrane Body Fluids Bile Ducts COS Cells

Organisms10

Rats, Mutant Strains Mice, Mutant Strains Mice, Transgenic Dogs Mice, Knockout Mice, Inbred C57BL Rats, Sprague-Dawley Fishes, Poisonous Escherichia coli Zebrafish

Diseases58

Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive Polycystic Ovary Syndrome Cysts Kidney Diseases, Cystic Kidney Diseases Hyperandrogenism Caroli Disease Kidney Failure, Chronic Disease Models, Animal Liver Diseases Retinitis Pigmentosa Hirsutism Syndrome Orofaciodigital Syndromes Disease Progression Oligomenorrhea Optic Atrophy, Autosomal Dominant Abnormalities, Multiple Tuberous Sclerosis Anovulation Kidney Neoplasms Genetic Predisposition to Disease Hematuria Cataract Kidney Calculi Hypertension, Renal CADASIL Acute Kidney Injury Ciliary Motility Disorders Spermatocele Multicystic Dysplastic Kidney Cerebellar Ataxia Infertility, Female Renal Insufficiency Spinocerebellar Degenerations Dementia, Multi-Infarct Spastic Paraplegia, Hereditary Proteinuria Hand Deformities, Congenital Hearing Loss, Sensorineural Hajdu-Cheney Syndrome Hypertension Foot Deformities, Congenital Ectodermal Dysplasia Insulin Resistance Chromosome Disorders Eye Diseases, Hereditary Intracranial Aneurysm Charcot-Marie-Tooth Disease Keratoderma, Palmoplantar Deafness Spinocerebellar Ataxias Menstruation Disturbances Nails, Malformed Eye Abnormalities Encephalocele

Chemicals and Drugs51

TRPP Cation Channels Proteins Membrane Proteins Genetic Markers Codon, Nonsense DNA Primers Receptors, Vasopressin RNA, Messenger Receptors, Cell Surface DNA Iothalamic Acid Metformin Eye Proteins Clomiphene Transcription Factors TOR Serine-Threonine Kinases Carrier Proteins Tumor Suppressor Proteins Nuclear Proteins Testosterone Creatinine Uromodulin DNA-Binding Proteins DNA, Complementary Androgens Recombinant Proteins Mutant Proteins gamma-Crystallins Codon Fertility Agents, Female Proto-Oncogene Proteins Protein-Serine-Threonine Kinases Proto-Oncogene Proteins B-raf Benzazepines Androstenedione Biological Markers beta-Crystallin A Chain Rhodopsin Luteinizing Hormone Sodium-Potassium-Exchanging ATPase Potassium Citrate Cystic Fibrosis Transmembrane Conductance Regulator Recombinant Fusion Proteins Cyclic AMP 17-alpha-Hydroxyprogesterone Repressor Proteins Sirolimus Cytoskeletal Proteins Calcium Follicle Stimulating Hormone RNA Splice Sites

Analytical, Diagnostic and Therapeutic Techniques and Equipment40

Pedigree DNA Mutational Analysis Kidney Transplantation Chromosome Mapping Disease Models, Animal Polymerase Chain Reaction Genetic Testing Amino Acid Substitution Sequence Analysis, DNA Kidney Function Tests Glomerular Filtration Rate Organ Size Immunohistochemistry Cloning, Molecular Mutagenesis, Site-Directed Transfection Sequence Alignment Nephrectomy Blotting, Western Models, Biological Models, Genetic Reverse Transcriptase Polymerase Chain Reaction Hand-Assisted Laparoscopy Case-Control Studies Models, Molecular Crosses, Genetic Tomography, X-Ray Computed Risk Factors Retrospective Studies Magnetic Resonance Imaging Electroretinography Treatment Outcome Prevalence Cohort Studies Ovulation Induction Reference Values Genetic Association Studies Fluorescent Antibody Technique Ultrasonography Heterozygote Detection

Psychiatry and Psychology2

Dementia, Multi-Infarct Family

Phenomena and Processes77

Genes, Dominant Mutation Mutation, Missense Point Mutation Genetic Linkage Frameshift Mutation Phenotype Chromosomes, Human, Pair 16 Heterozygote Base Sequence Lod Score Exons Germ-Line Mutation Genes, Recessive Genotype Alleles Amino Acid Sequence Polymorphism, Single-Stranded Conformational Genetic Markers Codon, Nonsense Homozygote Amino Acid Substitution Signal Transduction Protein Structure, Tertiary Glomerular Filtration Rate Polymorphism, Genetic Anovulation Haplotypes Sequence Deletion Genetic Predisposition to Disease Organ Size Genetic Heterogeneity Penetrance Mutation Rate Sequence Homology, Amino Acid Gene Deletion Time Factors Microsatellite Repeats Transfection Chromosomes, Human, Pair 4 Cell Proliferation Gene Expression Gene Expression Regulation Protein Binding Polymorphism, Restriction Fragment Length Pregnancy Mutagenesis Introns Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 19 Founder Effect Genetic Variation Chromosomes, Human, Pair 6 Codon Consanguinity Exome Gene Frequency Transcription, Genetic Protein Transport Insulin Resistance Binding Sites Cell Polarity Apoptosis Chromosomes, Human, Pair 1 Suppression, Genetic Phosphorylation Polymorphism, Single Nucleotide Recombination, Genetic Loss of Heterozygosity Protein Conformation Tissue Distribution Gene Expression Regulation, Developmental Renal Circulation Cell Division Conserved Sequence Promoter Regions, Genetic RNA Splice Sites

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups2

Infant, Newborn Asian Continental Ancestry Group

Health Care10

Genetic Testing Age of Onset Family Health Case-Control Studies Genetic Counseling Risk Factors Retrospective Studies Treatment Outcome Prevalence Cohort Studies

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

Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant TRPP Cation Channels Polycystic Kidney, Autosomal Recessive Polycystic Ovary Syndrome Genes, Dominant Kidney Pedigree Cysts Mutation Mutation, Missense Point Mutation Cilia Kidney Diseases, Cystic Genetic Linkage Frameshift Mutation Kidney Tubules DNA Mutational Analysis Phenotype Kidney Diseases Molecular Sequence Data Chromosomes, Human, Pair 16 Heterozygote Hyperandrogenism Caroli Disease Base Sequence Lod Score Exons Germ-Line Mutation Kidney Transplantation Chromosome Mapping Kidney Failure, Chronic Cyst Fluid Disease Models, Animal Liver Diseases Genes, Recessive Retinitis Pigmentosa Genotype Proteins Hirsutism Polymerase Chain Reaction Alleles Amino Acid Sequence Membrane Proteins Syndrome Rats, Mutant Strains Polymorphism, Single-Stranded Conformational Orofaciodigital Syndromes Genetic Testing Age of Onset Genetic Markers Cell Line Codon, Nonsense Disease Progression Kidney Cortex Homozygote Amino Acid Substitution Kidney Tubules, Collecting Oligomenorrhea Family Health Optic Atrophy, Autosomal Dominant Sequence Analysis, DNA Kidney Function Tests Abnormalities, Multiple Tuberous Sclerosis Signal Transduction Epithelial Cells DNA Primers Protein Structure, Tertiary Mice, Mutant Strains Kidney Tubules, Proximal Glomerular Filtration Rate Polymorphism, Genetic Anovulation Haplotypes Receptors, Vasopressin Kidney Neoplasms Sequence Deletion Genetic Predisposition to Disease RNA, Messenger Organ Size Hematuria Cataract Kidney Calculi Receptors, Cell Surface Genetic Heterogeneity Penetrance Mutation Rate DNA Sequence Homology, Amino Acid Gene Deletion Iothalamic Acid Cells, Cultured Mice, Transgenic Kidney Glomerulus Metformin Hypertension, Renal Immunohistochemistry CADASIL Eye Proteins

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