Liver polycystic kidney autosomal recessive. Medical search. Frequent questions

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Anatomy29

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

Organisms9

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

Diseases84

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

Chemicals and Drugs36

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

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

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes58

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

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups2

Infant, Newborn Arabs

Health Care11

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

Geographicals1

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

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