Involvement renal disease genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy17

Fundus Oculi Retina Photoreceptor Cells, Vertebrate Pigment Epithelium of Eye Photoreceptor Cells Retinal Pigment Epithelium Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Kidney Chromosomes, Human, Pair 4 Muscle, Skeletal Kidney Glomerulus Rod Cell Outer Segment X Chromosome Cells, Cultured Chromosomes, Human, Pair 5 Kidney Tubules

Organisms4

Mice, Inbred mdx Rats, Mutant Strains Mice, Inbred C57BL Mice, Knockout

Diseases69

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Kidney Failure, Chronic Muscular Dystrophy, Animal Genetic Diseases, Inborn Retinal Diseases Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Kidney Diseases Eye Diseases, Hereditary Disease Blindness Muscular Dystrophy, Facioscapulohumeral Bardet-Biedl Syndrome Kidney Diseases, Cystic Microphthalmos Syndrome Night Blindness Alstrom Syndrome Muscular Dystrophy, Emery-Dreifuss Macular Degeneration Optic Atrophy, Hereditary, Leber Usher Syndromes Choroid Diseases Optic Atrophies, Hereditary Neuroaxonal Dystrophies Proteinuria Optic Disk Drusen Disease Models, Animal Diabetic Nephropathies Genetic Predisposition to Disease Abnormalities, Multiple Intellectual Disability Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Glomerulonephritis Vision Disorders Hepatolenticular Degeneration Vitelliform Macular Dystrophy Huntington Disease Disease Progression Renal Insufficiency, Chronic Polycystic Kidney Diseases Lupus Nephritis Neuromuscular Diseases Nephritis, Interstitial AIDS-Associated Nephropathy Nephritis Albuminuria Glomerulosclerosis, Focal Segmental Renal Insufficiency Polycystic Kidney, Autosomal Dominant Machado-Joseph Disease Nephrosclerosis Hypertension, Renal Uremia Chronic Disease Glomerulonephritis, IGA Myotonic Disorders Fibrosis Menkes Kinky Hair Syndrome Cardiomyopathies Hypertension

Chemicals and Drugs26

cis-trans-Isomerases Eye Proteins Peripherins Dystrophin Codon, Nonsense Genetic Markers Nerve Tissue Proteins Proteins Sarcoglycans Lipofuscin Carrier Proteins Membrane Proteins Rhodopsin Creatinine Dystroglycans Utrophin Intermediate Filament Proteins ATP-Binding Cassette Transporters Rod Opsins Guanylate Cyclase RNA, Messenger Thymopoietins Collagen Type VI Receptor Protein-Tyrosine Kinases DNA Biological Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment34

Electroretinography Pedigree DNA Mutational Analysis Chromosome Mapping Renal Dialysis Visual Acuity Fluorescein Angiography Genetic Testing Glomerular Filtration Rate Disease Models, Animal Heteroduplex Analysis Tomography, Optical Coherence Polymerase Chain Reaction Visual Field Tests Ophthalmoscopy Sequence Analysis, DNA Kidney Transplantation Models, Genetic Kidney Function Tests Heterozygote Detection Risk Factors Renal Replacement Therapy Protein Interaction Mapping Peritoneal Dialysis Retrospective Studies Genetic Association Studies Genome-Wide Association Study Gene Expression Profiling Biopsy Amino Acid Substitution Case-Control Studies Cohort Studies Follow-Up Studies Treatment Outcome

Psychiatry and Psychology5

Visual Acuity Visual Fields Intellectual Disability Huntington Disease Vision, Ocular

Phenomena and Processes52

Genes, Recessive Consanguinity Mutation Genetic Linkage Phenotype Genes, Dominant Lod Score Mutation, Missense Exome Visual Acuity Exons Dark Adaptation Haplotypes Homozygote Codon, Nonsense Base Sequence Genetic Markers Genotype Heterozygote Glomerular Filtration Rate Visual Fields Genetic Predisposition to Disease Frameshift Mutation Polymorphism, Single-Stranded Conformational Amino Acid Sequence Polymorphism, Single Nucleotide Genome, Human Chromosomes, Human, Pair 4 Alleles Trinucleotide Repeat Expansion Point Mutation Linkage Disequilibrium Genetic Heterogeneity Time Factors X Chromosome Protein Interaction Maps Gene Regulatory Networks Vision, Ocular Algorithms Amino Acid Substitution Polymorphism, Genetic Light Gene Frequency Genetic Structures Chromosomes, Human, Pair 5 Genes Fluorescence Founder Effect Gene Expression Regulation Microsatellite Repeats Penetrance Gene Deletion

Disciplines and Occupations3

Computational Biology Nephrology Genetics, Medical

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Databases, Genetic Algorithms

Health Care9

Age of Onset Genetic Testing Risk Factors Retrospective Studies Genome-Wide Association Study Case-Control Studies Cohort Studies Follow-Up Studies Treatment Outcome

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Health Care

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Electroretinography Pedigree cis-trans-Isomerases Eye Proteins Kidney Failure, Chronic Muscular Dystrophy, Animal Fundus Oculi Genes, Recessive Consanguinity Genetic Diseases, Inborn Retinal Diseases Mutation Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Kidney Diseases Eye Diseases, Hereditary DNA Mutational Analysis Genetic Linkage Retina Disease Photoreceptor Cells, Vertebrate Chromosome Mapping Phenotype Peripherins Blindness Muscular Dystrophy, Facioscapulohumeral Genes, Dominant Dystrophin Bardet-Biedl Syndrome Kidney Diseases, Cystic Pigment Epithelium of Eye Renal Dialysis Microphthalmos Photoreceptor Cells Syndrome Lod Score Night Blindness Mutation, Missense Exome Alstrom Syndrome Visual Acuity Exons Molecular Sequence Data Dark Adaptation Retinal Pigment Epithelium Haplotypes Muscular Dystrophy, Emery-Dreifuss Fluorescein Angiography Macular Degeneration Mice, Inbred mdx Homozygote Retinal Rod Photoreceptor Cells Codon, Nonsense Optic Atrophy, Hereditary, Leber Base Sequence Usher Syndromes Genetic Markers Genotype Age of Onset Heterozygote Genetic Testing Nerve Tissue Proteins Retinal Cone Photoreceptor Cells Choroid Diseases Optic Atrophies, Hereditary Neuroaxonal Dystrophies Proteins Proteinuria Kidney Rats, Mutant Strains Optic Disk Drusen Sarcoglycans Glomerular Filtration Rate Disease Models, Animal Lipofuscin Diabetic Nephropathies Visual Fields Genetic Predisposition to Disease Frameshift Mutation Carrier Proteins Polymorphism, Single-Stranded Conformational Abnormalities, Multiple Intellectual Disability Heteroduplex Analysis Membrane Proteins Amino Acid Sequence Polymorphism, Single Nucleotide Tomography, Optical Coherence Rhodopsin Creatinine Polymerase Chain Reaction Muscular Dystrophy, Oculopharyngeal

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