Incidence polycystic kidney autosomal recessive. Medical search. Frequent questions

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Anatomy25

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 Chromosomes, Human, Pair 6 Epithelium Kidney Medulla Chromosomes, Human, Pair 1 Bile Ducts Chromosomes, Human, Pair 19 Body Fluids Ureter

Organisms8

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

Diseases84

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

Chemicals and Drugs39

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment44

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

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes57

Genes, Recessive Consanguinity Mutation Homozygote Phenotype Genetic Linkage Chromosomes, Human, Pair 16 Heterozygote Mutation, Missense 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 Time Factors Pregnancy Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Signal Transduction Genetic Heterogeneity Point Mutation Genetic Predisposition to Disease Founder Effect Cell Proliferation Microsatellite Repeats Chromosomes, Human, Pair 4 Sequence Deletion Gene Deletion Exome Insulin Resistance Chromosomes, Human, Pair 2 Sequence Homology, Amino Acid Chromosomes, Human, Pair 6 Protein Structure, Tertiary Gene Expression Chromosomes, Human, Pair 1 Gene Expression Regulation Introns Tissue Distribution Cell Polarity Gene Frequency Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 19 Blood Pressure Polymorphism, Single Nucleotide Renal Circulation Chromosome Aberrations Apoptosis

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science6

Incidence Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence Registries

Named Groups3

Infant, Newborn Arabs Jews

Health Care15

Incidence Genetic Testing Risk Factors Age of Onset Family Health Retrospective Studies Treatment Outcome Cohort Studies Case-Control Studies Follow-Up Studies Prospective Studies Prevalence Genetic Counseling Severity of Illness Index Registries

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

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