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

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Anatomy23

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

Organisms5

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

Diseases67

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

Chemicals and Drugs26

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment38

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

Psychiatry and Psychology5

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular Huntington Disease

Phenomena and Processes52

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

Disciplines and Occupations4

Computational Biology Immunohistochemistry Nephrology Genetics, Medical

Information Science5

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

Health Care8

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

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

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