Congenital polycystic kidney autosomal dominant. Medical search. Frequent questions

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Anatomy28

Kidney Cilia Kidney Tubules Chromosomes, Human, Pair 16 Cyst Fluid Kidney Cortex Kidney Tubules, Collecting Kidney Tubules, Proximal Epithelial Cells Cell Line Kidney Glomerulus Nephrons Chromosomes, Human, Pair 4 Ovary Cells, Cultured Kidney Medulla Liver Chromosomes, Human, Pair 6 Epithelium Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 19 Body Fluids Bile Ducts Chromosomes, Human, Pair 1 Ureter Colon, Descending Cell Membrane Chromosomes, Human, Pair 12

Organisms9

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

Diseases64

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 Liver Diseases Hirsutism Disease Models, Animal Retinitis Pigmentosa Orofaciodigital Syndromes Oligomenorrhea Disease Progression Optic Atrophy, Autosomal Dominant Tuberous Sclerosis Syndrome Anovulation Hematuria Kidney Calculi Kidney Neoplasms Abnormalities, Multiple Hypertension, Renal Acute Kidney Injury Cataract CADASIL Spermatocele Ciliary Motility Disorders Multicystic Dysplastic Kidney Infertility, Female Renal Insufficiency Spinocerebellar Degenerations Proteinuria Dementia, Multi-Infarct Genetic Predisposition to Disease Cerebellar Ataxia Hajdu-Cheney Syndrome Hypertension Spastic Paraplegia, Hereditary Insulin Resistance Hand Deformities, Congenital Intracranial Aneurysm Chromosome Disorders Foot Deformities, Congenital Menstruation Disturbances Nails, Malformed Hearing Loss, Sensorineural Encephalocele Spinocerebellar Ataxias Ectodermal Dysplasia Pancreatic Cyst Keratoderma, Palmoplantar Eye Diseases, Hereditary Mouth Abnormalities Acne Vulgaris Charcot-Marie-Tooth Disease Syndactyly Albuminuria Amenorrhea Epilepsy, Frontal Lobe Telangiectasia, Hereditary Hemorrhagic

Chemicals and Drugs49

TRPP Cation Channels Proteins Genetic Markers Membrane Proteins Receptors, Vasopressin Iothalamic Acid Metformin Receptors, Cell Surface Clomiphene TOR Serine-Threonine Kinases RNA, Messenger Codon, Nonsense Testosterone Creatinine Uromodulin DNA Primers Androgens Eye Proteins Fertility Agents, Female Androstenedione Benzazepines DNA Biological Markers Potassium Citrate Luteinizing Hormone Tumor Suppressor Proteins gamma-Crystallins Sodium-Potassium-Exchanging ATPase 17-alpha-Hydroxyprogesterone beta-Crystallin A Chain Sirolimus Follicle Stimulating Hormone Cyclic AMP Rhodopsin Cyproterone Acetate Vasopressins DNA, Complementary Dehydroepiandrosterone Sulfate Carrier Proteins Protein-Serine-Threonine Kinases Transcription Factors Immunosuppressive Agents Calcium DNA, Satellite Aquaporin 2 Insulin Peripherins Alpha-Globulins Sex Hormone-Binding Globulin

Analytical, Diagnostic and Therapeutic Techniques and Equipment44

Pedigree Kidney Transplantation DNA Mutational Analysis Disease Models, Animal Chromosome Mapping Kidney Function Tests Glomerular Filtration Rate Organ Size Genetic Testing Polymerase Chain Reaction Nephrectomy Hand-Assisted Laparoscopy Immunohistochemistry Tomography, X-Ray Computed Sequence Analysis, DNA Blotting, Western Models, Biological Case-Control Studies Retrospective Studies Magnetic Resonance Imaging Risk Factors Treatment Outcome Reverse Transcriptase Polymerase Chain Reaction Ovulation Induction Ultrasonography Prevalence Amino Acid Substitution Cloning, Molecular Transfection Blood Pressure Crosses, Genetic Electroretinography Blood Urea Nitrogen Reference Values Renal Dialysis Sequence Alignment Fluorescent Antibody Technique Models, Genetic Severity of Illness Index Follow-Up Studies Cohort Studies Prospective Studies In Situ Hybridization Molecular Diagnostic Techniques

Psychiatry and Psychology2

Dementia, Multi-Infarct Family

Phenomena and Processes62

Genes, Dominant Mutation Genetic Linkage Chromosomes, Human, Pair 16 Lod Score Phenotype Mutation, Missense Heterozygote Genetic Markers Base Sequence Genes, Recessive Exons Glomerular Filtration Rate Anovulation Haplotypes Genotype Organ Size Frameshift Mutation Amino Acid Sequence Signal Transduction Alleles Chromosomes, Human, Pair 4 Genetic Heterogeneity Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Penetrance Time Factors Codon, Nonsense Cell Proliferation Homozygote Pregnancy Genetic Predisposition to Disease Point Mutation Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 19 Protein Structure, Tertiary Insulin Resistance Gene Expression Microsatellite Repeats Gene Expression Regulation Cell Polarity Gene Deletion Sequence Deletion Sequence Homology, Amino Acid Polymorphism, Restriction Fragment Length Renal Circulation Germ-Line Mutation Amino Acid Substitution Transfection Blood Pressure Chromosomes, Human, Pair 1 Tissue Distribution Renal Blood Flow, Effective Apoptosis Renin-Angiotensin System Protein Transport Ovulation Chromosomes, Human, Pair 12 DNA, Satellite Protein Binding Organ Specificity

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care14

Age of Onset Family Health Genetic Testing Case-Control Studies Genetic Counseling Retrospective Studies Risk Factors Treatment Outcome Prevalence Severity of Illness Index Follow-Up Studies Age Factors Cohort Studies Prospective 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 Cysts Pedigree Cilia Kidney Diseases, Cystic Mutation Kidney Tubules Genetic Linkage Kidney Diseases Chromosomes, Human, Pair 16 Hyperandrogenism Caroli Disease Kidney Transplantation Lod Score Kidney Failure, Chronic Cyst Fluid Phenotype Liver Diseases DNA Mutational Analysis Hirsutism Disease Models, Animal Mutation, Missense Molecular Sequence Data Retinitis Pigmentosa Rats, Mutant Strains Chromosome Mapping Orofaciodigital Syndromes Proteins Kidney Cortex Kidney Tubules, Collecting Oligomenorrhea Heterozygote Kidney Function Tests Disease Progression Optic Atrophy, Autosomal Dominant Genetic Markers Base Sequence Genes, Recessive Age of Onset Exons Membrane Proteins Tuberous Sclerosis Kidney Tubules, Proximal Syndrome Glomerular Filtration Rate Epithelial Cells Anovulation Haplotypes Receptors, Vasopressin Genotype Hematuria Organ Size Frameshift Mutation Kidney Calculi Kidney Neoplasms Family Health Abnormalities, Multiple Iothalamic Acid Cell Line Metformin Hypertension, Renal Kidney Glomerulus Amino Acid Sequence Genetic Testing Receptors, Cell Surface Acute Kidney Injury Cataract Nephrons Signal Transduction CADASIL Clomiphene Mice, Mutant Strains Alleles Spermatocele Polymerase Chain Reaction Nephrectomy Ciliary Motility Disorders Chromosomes, Human, Pair 4 Multicystic Dysplastic Kidney Dogs Genetic Heterogeneity Hand-Assisted Laparoscopy Ovary TOR Serine-Threonine Kinases Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Infertility, Female Renal Insufficiency RNA, Messenger Penetrance Immunohistochemistry Mice, Transgenic Spinocerebellar Degenerations Time Factors

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