Hereditary disease genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy13

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

Organisms4

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

Diseases46

Retinal Dystrophies Genetic Diseases, Inborn Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Nephritis, Hereditary Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Genetic Predisposition to Disease Retinal Diseases Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Eye Diseases, Hereditary Disease Blindness Muscular Dystrophy, Facioscapulohumeral Bardet-Biedl Syndrome Microphthalmos Night Blindness Alstrom Syndrome Syndrome Muscular Dystrophy, Emery-Dreifuss Macular Degeneration Kidney Diseases, Cystic Usher Syndromes Optic Atrophy, Hereditary, Leber Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Optic Disk Drusen Intellectual Disability Abnormalities, Multiple Muscular Dystrophy, Oculopharyngeal Reflex Sympathetic Dystrophy Vision Disorders Hepatolenticular Degeneration Vitelliform Macular Dystrophy Huntington Disease Disease Models, Animal Neuromuscular Diseases Machado-Joseph Disease Myotonic Disorders Menkes Kinky Hair Syndrome

Chemicals and Drugs23

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Pedigree DNA Mutational Analysis Genetic Testing Electroretinography Chromosome Mapping Visual Acuity Fluorescein Angiography Heteroduplex Analysis Tomography, Optical Coherence Visual Field Tests Ophthalmoscopy Polymerase Chain Reaction Disease Models, Animal Sequence Analysis, DNA Models, Genetic Heterozygote Detection Protein Interaction Mapping Amino Acid Substitution Genetic Association Studies Genome-Wide Association Study Gene Expression Profiling

Psychiatry and Psychology5

Visual Acuity Visual Fields Intellectual Disability Huntington Disease Vision, Ocular

Phenomena and Processes47

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

Disciplines and Occupations2

Computational Biology Genetics, Medical

Information Science5

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

Health Care3

Genetic Testing Age of Onset Genome-Wide Association Study

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 Genetic Diseases, Inborn Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Pedigree Mutation Leber Congenital Amaurosis Nephritis, Hereditary Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary DNA Mutational Analysis Genetic Testing Electroretinography cis-trans-Isomerases Chromosome Mapping Phenotype Trinucleotide Repeats Eye Proteins Muscular Dystrophy, Animal Fundus Oculi Genes, Recessive Genetic Predisposition to Disease Molecular Sequence Data Consanguinity Retinal Diseases Base Sequence Fuchs' Endothelial Dystrophy Laurence-Moon Syndrome Eye Diseases, Hereditary Disease Retina Genetic Linkage Photoreceptor Cells, Vertebrate Amino Acid Sequence Peripherins Blindness DNA Muscular Dystrophy, Facioscapulohumeral Genes, Dominant Dystrophin DNA Repair Pigment Epithelium of Eye Bardet-Biedl Syndrome Microphthalmos Photoreceptor Cells Night Blindness Lod Score Mutation, Missense Exome Alstrom Syndrome Dark Adaptation Syndrome Visual Acuity Retinal Pigment Epithelium Exons Haplotypes Muscular Dystrophy, Emery-Dreifuss Macular Degeneration Kidney Diseases, Cystic Fluorescein Angiography Mice, Inbred mdx Retinal Rod Photoreceptor Cells Codon, Nonsense Usher Syndromes Optic Atrophy, Hereditary, Leber Homozygote Retinal Cone Photoreceptor Cells Genetic Markers Choroid Diseases Neuroaxonal Dystrophies Nerve Tissue Proteins Optic Atrophies, Hereditary Heterozygote Optic Disk Drusen Sarcoglycans Age of Onset Lipofuscin Rats, Mutant Strains Genotype Visual Fields Proteins Frameshift Mutation Polymorphism, Single-Stranded Conformational Heteroduplex Analysis Intellectual Disability Abnormalities, Multiple Tomography, Optical Coherence Rhodopsin Carrier Proteins Muscular Dystrophy, Oculopharyngeal Dystroglycans Visual Field Tests Reflex Sympathetic Dystrophy Databases, Genetic Chromosomes, Human, Pair 4 Polymorphism, Single Nucleotide Genome, Human Membrane Proteins

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