Kidneys polycystic kidney autosomal dominant. Medical search. Frequent questions

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Anatomy29

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

Organisms9

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

Diseases64

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

Chemicals and Drugs51

TRPP Cation Channels Proteins Membrane Proteins Genetic Markers Receptors, Vasopressin Iothalamic Acid Creatinine Receptors, Cell Surface Metformin RNA, Messenger Clomiphene TOR Serine-Threonine Kinases Uromodulin Testosterone Codon, Nonsense DNA Primers Biological Markers DNA Androgens Eye Proteins Benzazepines Fertility Agents, Female Sodium-Potassium-Exchanging ATPase Androstenedione Potassium Citrate Tumor Suppressor Proteins Immunosuppressive Agents Luteinizing Hormone DNA, Complementary gamma-Crystallins Sirolimus Carrier Proteins Cyclic AMP 17-alpha-Hydroxyprogesterone beta-Crystallin A Chain Vasopressins Follicle Stimulating Hormone Aquaporin 2 Calcium Rhodopsin Transcription Factors Cyproterone Acetate Protein-Serine-Threonine Kinases Dehydroepiandrosterone Sulfate Recombinant Proteins Alpha-Globulins Insulin Hepatocyte Nuclear Factor 1-beta Nuclear Proteins DNA, Satellite Chlorides

Analytical, Diagnostic and Therapeutic Techniques and Equipment44

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

Psychiatry and Psychology2

Dementia, Multi-Infarct Family

Phenomena and Processes66

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

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 Risk Factors Retrospective Studies Treatment Outcome Case-Control Studies Genetic Counseling Prevalence Follow-Up Studies Severity of Illness Index Prospective Studies Cohort Studies Age Factors

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

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