Organs polycystic kidney autosomal dominant. Medical search. Frequent questions

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Anatomy29

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

Organisms9

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

Diseases65

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 Disease Models, Animal Hirsutism Retinitis Pigmentosa Orofaciodigital Syndromes Oligomenorrhea Disease Progression Optic Atrophy, Autosomal Dominant Tuberous Sclerosis Syndrome Anovulation Hematuria Kidney Neoplasms Kidney Calculi Abnormalities, Multiple Hypertension, Renal Acute Kidney Injury Cataract CADASIL Spermatocele Ciliary Motility Disorders Multicystic Dysplastic Kidney Renal Insufficiency Infertility, Female Spinocerebellar Degenerations Proteinuria Genetic Predisposition to Disease Dementia, Multi-Infarct Cerebellar Ataxia Hypertension Hajdu-Cheney Syndrome Spastic Paraplegia, Hereditary Insulin Resistance Hand Deformities, Congenital Intracranial Aneurysm Chromosome Disorders Foot Deformities, Congenital Nails, Malformed Menstruation Disturbances Hearing Loss, Sensorineural Encephalocele Spinocerebellar Ataxias Multiple Organ Failure Ectodermal Dysplasia Pancreatic Cyst Keratoderma, Palmoplantar Eye Diseases, Hereditary Mouth Abnormalities Acne Vulgaris Albuminuria Charcot-Marie-Tooth Disease Syndactyly 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 RNA, Messenger TOR Serine-Threonine Kinases Testosterone Creatinine Codon, Nonsense DNA Primers Uromodulin Eye Proteins Androgens Fertility Agents, Female DNA Androstenedione Benzazepines Biological Markers Tumor Suppressor Proteins Luteinizing Hormone Potassium Citrate gamma-Crystallins Sodium-Potassium-Exchanging ATPase 17-alpha-Hydroxyprogesterone beta-Crystallin A Chain Sirolimus Follicle Stimulating Hormone DNA, Complementary Cyclic AMP Rhodopsin Transcription Factors Immunosuppressive Agents Carrier Proteins Cyproterone Acetate Vasopressins Dehydroepiandrosterone Sulfate Protein-Serine-Threonine Kinases Calcium Nuclear Proteins Insulin DNA, Satellite Alpha-Globulins Aquaporin 2 Anti-Mullerian Hormone

Analytical, Diagnostic and Therapeutic Techniques and Equipment45

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

Psychiatry and Psychology2

Dementia, Multi-Infarct Family

Phenomena and Processes65

Genes, Dominant Mutation Genetic Linkage Chromosomes, Human, Pair 16 Phenotype Lod Score Mutation, Missense Organ Size Heterozygote Base Sequence Genetic Markers Genes, Recessive Exons Glomerular Filtration Rate Anovulation Haplotypes Genotype Frameshift Mutation Amino Acid Sequence Signal Transduction Alleles Chromosomes, Human, Pair 4 Time Factors Organ Specificity Genetic Heterogeneity Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Cell Proliferation Pregnancy Penetrance Codon, Nonsense Homozygote Genetic Predisposition to Disease Point Mutation Gene Expression Chromosomes, Human, Pair 6 Gene Expression Regulation Chromosomes, Human, Pair 2 Protein Structure, Tertiary Chromosomes, Human, Pair 19 Tissue Distribution Insulin Resistance Cell Polarity Microsatellite Repeats Sequence Homology, Amino Acid Gene Deletion Sequence Deletion Renal Circulation Polymorphism, Restriction Fragment Length Blood Pressure Transfection Amino Acid Substitution Germ-Line Mutation Chromosomes, Human, Pair 1 Renal Blood Flow, Effective Gene Expression Regulation, Developmental Apoptosis Renin-Angiotensin System Protein Transport Ovulation Cell Division Protein Binding 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 Care15

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

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