Emphasis 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 Epithelium Chromosomes, Human, Pair 2 Kidney Medulla Chromosomes, Human, Pair 6 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

Diseases85

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 Kidney Neoplasms Ichthyosiform Erythroderma, Congenital Acute Kidney Injury Hematuria Intellectual Disability Hypertension, Renal Multicystic Dysplastic Kidney Ichthyosis, Lamellar Deafness Encephalocele Infertility, Female Dwarfism 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 Hypertension Mouth Abnormalities Chromosome Disorders 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 Genetic Diseases, Inborn Microphthalmos Fetal Diseases Optic Atrophy Foot Deformities, Congenital Eye Abnormalities Intracranial Aneurysm Hair Diseases Acidosis, Renal Tubular Syndactyly Spastic Paraplegia, Hereditary Muscle Hypotonia Spinal Muscular Atrophies of Childhood Hand Deformities, Congenital Fanconi Anemia Granulomatous Disease, Chronic Acne Vulgaris

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 TOR Serine-Threonine Kinases Creatinine DNA Androgens Fertility Agents, Female Androstenedione Biological Markers Potassium Citrate Sarcoglycans Eye Proteins Carrier Proteins Luteinizing Hormone DNA, Complementary Aquaporin 2 17-alpha-Hydroxyprogesterone 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

Analytical, Diagnostic and Therapeutic Techniques and Equipment40

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 Sequence Analysis, DNA Crosses, Genetic Heterozygote Detection Models, Biological Case-Control Studies Tomography, X-Ray Computed Prenatal Diagnosis Blotting, Western Retrospective Studies Risk Factors Treatment Outcome Cloning, Molecular Reverse Transcriptase Polymerase Chain Reaction Magnetic Resonance Imaging Sequence Alignment Models, Genetic Ovulation Induction Electroretinography Reference Values Prevalence Blood Urea Nitrogen Ultrasonography Fluorescent Antibody Technique Blood Pressure Renal Dialysis Cohort Studies Follow-Up Studies

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes57

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

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 Care11

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

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