Syndromes polycystic kidney autosomal recessive. Medical search. Frequent questions

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Anatomy23

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 Cells, Cultured Ovary Liver Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 6 Epithelium Chromosomes, Human, Pair 1 Kidney Medulla Bile Ducts Chromosomes, Human, Pair 19

Organisms8

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

Diseases99

Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive Polycystic Ovary Syndrome Syndrome Cysts Kidney Diseases, Cystic Caroli Disease Kidney Diseases Abnormalities, Multiple Hyperandrogenism Disease Models, Animal Kidney Failure, Chronic Orofaciodigital Syndromes Hirsutism Liver Diseases Metabolic Syndrome X Retinitis Pigmentosa Microcephaly Oligomenorrhea Down Syndrome Disease Progression Ciliary Motility Disorders Ichthyosis Intellectual Disability Anovulation Hypotrichosis Nephrotic Syndrome Ichthyosiform Erythroderma, Congenital Kidney Calculi Kidney Neoplasms Acute Kidney Injury Hematuria Dwarfism Encephalocele Deafness Hearing Loss, Sensorineural Sjogren's Syndrome Hypertension, Renal Multicystic Dysplastic Kidney Infertility, Female Genetic Predisposition to Disease Ichthyosis, Lamellar Osteochondrodysplasias Cerebellar Ataxia Insulin Resistance Bone Diseases, Developmental Proteinuria Muscular Dystrophies Renal Insufficiency Spermatocele Tuberous Sclerosis Chromosome Disorders Facies Werner Syndrome Nails, Malformed Eye Abnormalities Ectodermal Dysplasia Mouth Abnormalities Metabolism, Inborn Errors Turner Syndrome Bloom Syndrome Eye Diseases, Hereditary Bardet-Biedl Syndrome Osteopetrosis Craniofacial Abnormalities Hand Deformities, Congenital Hypertension Syndactyly Usher Syndromes Foot Deformities, Congenital Hajdu-Cheney Syndrome Albinism, Oculocutaneous Muscle Hypotonia Myelodysplastic Syndromes Charcot-Marie-Tooth Disease Fetal Diseases Menstruation Disturbances Cushing Syndrome Hearing Loss Microphthalmos Cutis Laxa Cystinosis Optic Atrophy Dysostoses Genetic Diseases, Inborn Immunologic Deficiency Syndromes Retinal Degeneration Friedreich Ataxia Acute Coronary Syndrome Muscular Atrophy, Spinal Hair Diseases Arthrogryposis Chromosome Aberrations Amino Acid Metabolism, Inborn Errors Chediak-Higashi Syndrome Acidosis, Renal Tubular Hermanski-Pudlak Syndrome Williams Syndrome

Chemicals and Drugs33

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

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

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes55

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 Codon, Nonsense Amino Acid Sequence Alleles Haplotypes Genetic Markers Anovulation Glomerular Filtration Rate Organ Size Pregnancy Polymorphism, Single-Stranded Conformational Polymorphism, Genetic Genetic Heterogeneity Time Factors Point Mutation Signal Transduction Genetic Predisposition to Disease Founder Effect Insulin Resistance Gene Deletion Chromosomes, Human, Pair 4 Sequence Deletion Microsatellite Repeats Cell Proliferation Exome Sequence Homology, Amino Acid Chromosomes, Human, Pair 2 Protein Structure, Tertiary Chromosomes, Human, Pair 6 Gene Expression Gene Expression Regulation Chromosomes, Human, Pair 1 Introns Tissue Distribution Polymorphism, Single Nucleotide Gene Frequency Cell Polarity Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 19 Chromosome Aberrations Blood Pressure

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence Fatal Outcome

Named Groups2

Infant, Newborn Arabs

Health Care14

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

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

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