Causes polycystic kidney autosomal recessive. Medical search. Frequent questions

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Anatomy26

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

Organisms9

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

Diseases86

Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive Polycystic Ovary Syndrome Cysts Kidney Diseases, Cystic Caroli Disease Kidney Diseases Hyperandrogenism Syndrome Kidney Failure, Chronic Liver Diseases Disease Models, Animal Hirsutism Abnormalities, Multiple Orofaciodigital Syndromes Retinitis Pigmentosa Oligomenorrhea Microcephaly Disease Progression Ciliary Motility Disorders Ichthyosis Anovulation Hypotrichosis Kidney Calculi Ichthyosiform Erythroderma, Congenital Kidney Neoplasms Acute Kidney Injury Hematuria Intellectual Disability Hypertension, Renal Multicystic Dysplastic Kidney Ichthyosis, Lamellar Deafness Encephalocele Dwarfism Infertility, Female Hearing Loss, Sensorineural Osteochondrodysplasias Cerebellar Ataxia Spermatocele Muscular Dystrophies Genetic Predisposition to Disease Renal Insufficiency Tuberous Sclerosis Proteinuria Osteopetrosis Bone Diseases, Developmental Eye Diseases, Hereditary Metabolism, Inborn Errors Insulin Resistance Albinism, Oculocutaneous Nails, Malformed Charcot-Marie-Tooth Disease Mouth Abnormalities Chromosome Disorders Hypertension Menstruation Disturbances Friedreich Ataxia Ectodermal Dysplasia Cystinosis Muscular Atrophy, Spinal Hajdu-Cheney Syndrome Cutis Laxa Dysostoses Hearing Loss Retinal Degeneration Amino Acid Metabolism, Inborn Errors Microphthalmos Optic Atrophy Foot Deformities, Congenital Eye Abnormalities Hair Diseases Fetal Diseases Acidosis, Renal Tubular Genetic Diseases, Inborn Intracranial Aneurysm Syndactyly Spastic Paraplegia, Hereditary Muscle Hypotonia Spinal Muscular Atrophies of Childhood Hand Deformities, Congenital Fanconi Anemia Granulomatous Disease, Chronic Acne Vulgaris Arthrogryposis

Chemicals and Drugs40

TRPP Cation Channels Proteins Membrane Proteins Codon, Nonsense Genetic Markers Metformin Receptors, Vasopressin Receptors, Cell Surface Clomiphene Iothalamic Acid RNA, Messenger DNA Primers Testosterone TOR Serine-Threonine Kinases Creatinine Androgens DNA Fertility Agents, Female Androstenedione Potassium Citrate Biological Markers Sarcoglycans Eye Proteins Luteinizing Hormone Aquaporin 2 DNA, Complementary 17-alpha-Hydroxyprogesterone Carrier Proteins Benzazepines Tumor Suppressor Proteins Cystic Fibrosis Transmembrane Conductance Regulator Survival of Motor Neuron 1 Protein Follicle Stimulating Hormone Sodium-Potassium-Exchanging ATPase Cyproterone Acetate Uromodulin Dehydroepiandrosterone Sulfate Sirolimus Cyclic AMP Cytoskeletal Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment39

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

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes56

Genes, Recessive Consanguinity Mutation Homozygote Genetic Linkage Phenotype Chromosomes, Human, Pair 16 Mutation, Missense Heterozygote Lod Score Genes, Dominant Exons Base Sequence Frameshift Mutation Genotype Codon, Nonsense Amino Acid Sequence Alleles Haplotypes Genetic Markers Anovulation Glomerular Filtration Rate Organ Size Polymorphism, Single-Stranded Conformational Pregnancy Polymorphism, Genetic Genetic Heterogeneity Signal Transduction Point Mutation Founder Effect Chromosomes, Human, Pair 4 Genetic Predisposition to Disease Cell Proliferation Microsatellite Repeats Sequence Deletion Time Factors Gene Deletion Exome Sequence Homology, Amino Acid Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Protein Structure, Tertiary Insulin Resistance Chromosomes, Human, Pair 1 Gene Expression Introns Gene Expression Regulation Cell Polarity Tissue Distribution Chromosomes, Human, Pair 19 Polymorphism, Restriction Fragment Length Renal Circulation Gene Frequency Polymorphism, Single Nucleotide Protein Transport Blood Pressure

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups3

Infant, Newborn Arabs Jews

Health Care10

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

Geographicals2

Pakistan Tunisia

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 Geographicals

Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive Genes, Recessive TRPP Cation Channels Polycystic Ovary Syndrome Kidney Cysts Consanguinity Pedigree Cilia Kidney Diseases, Cystic Mutation Kidney Tubules Caroli Disease Homozygote Kidney Diseases Genetic Linkage Phenotype Hyperandrogenism DNA Mutational Analysis Chromosomes, Human, Pair 16 Kidney Transplantation Syndrome Kidney Failure, Chronic Chromosome Mapping Liver Diseases Disease Models, Animal Hirsutism Molecular Sequence Data Mutation, Missense Heterozygote Abnormalities, Multiple Cyst Fluid Lod Score Rats, Mutant Strains Genes, Dominant Orofaciodigital Syndromes Exons Proteins Retinitis Pigmentosa Base Sequence Kidney Tubules, Collecting Oligomenorrhea Frameshift Mutation Kidney Cortex Membrane Proteins Genotype Microcephaly Codon, Nonsense Amino Acid Sequence Kidney Function Tests Alleles Disease Progression Haplotypes Genetic Markers Mice, Mutant Strains Ciliary Motility Disorders Ichthyosis Kidney Tubules, Proximal Anovulation Hypotrichosis Genetic Testing Age of Onset Epithelial Cells Glomerular Filtration Rate Organ Size Kidney Calculi Metformin Receptors, Vasopressin Kidney Glomerulus Ichthyosiform Erythroderma, Congenital Kidney Neoplasms Family Health Cell Line Acute Kidney Injury Nephrons Dogs Receptors, Cell Surface Hematuria Polymorphism, Single-Stranded Conformational Clomiphene Polymerase Chain Reaction Intellectual Disability Hypertension, Renal Pakistan Iothalamic Acid Multicystic Dysplastic Kidney Infant, Newborn Pregnancy Polymorphism, Genetic RNA, Messenger Nephrectomy Ichthyosis, Lamellar Hand-Assisted Laparoscopy Deafness Encephalocele Ovary Dwarfism Infertility, Female

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