Onset hereditary genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy10

Fundus Oculi Photoreceptor Cells, Vertebrate Retina Pigment Epithelium of Eye Photoreceptor Cells Retinal Pigment Epithelium Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Muscle, Skeletal Rod Cell Outer Segment

Organisms4

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

Diseases37

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

Chemicals and Drugs21

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Heteroduplex Analysis Tomography, Optical Coherence Visual Field Tests Chromosome Mapping Ophthalmoscopy Genetic Testing Disease Models, Animal Polymerase Chain Reaction

Psychiatry and Psychology4

Visual Acuity Visual Fields Intellectual Disability Vision, Ocular

Phenomena and Processes27

Consanguinity Genes, Recessive Mutation Dark Adaptation Visual Acuity Genes, Dominant Phenotype Mutation, Missense Codon, Nonsense Exons Visual Fields Genetic Linkage Exome Homozygote Heterozygote Polymorphism, Single-Stranded Conformational Lod Score Frameshift Mutation Haplotypes Base Sequence Genotype Amino Acid Sequence Vision, Ocular Point Mutation Light Trinucleotide Repeat Expansion Fluorescence

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Age of Onset Genetic Testing

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

Retinal Dystrophies Muscular Dystrophies Retinal Degeneration Myotonic Dystrophy Leber Congenital Amaurosis Muscular Dystrophy, Duchenne Retinitis Pigmentosa Corneal Dystrophies, Hereditary Electroretinography cis-trans-Isomerases Muscular Dystrophy, Animal Eye Proteins Fundus Oculi Pedigree Fuchs' Endothelial Dystrophy Consanguinity Retinal Diseases Laurence-Moon Syndrome Genes, Recessive Eye Diseases, Hereditary Photoreceptor Cells, Vertebrate Retina Peripherins Blindness Muscular Dystrophy, Facioscapulohumeral Dystrophin Mutation DNA Mutational Analysis Pigment Epithelium of Eye Bardet-Biedl Syndrome Microphthalmos Photoreceptor Cells Night Blindness Alstrom Syndrome Dark Adaptation Visual Acuity Retinal Pigment Epithelium Genes, Dominant Muscular Dystrophy, Emery-Dreifuss Fluorescein Angiography Mice, Inbred mdx Syndrome Retinal Rod Photoreceptor Cells Phenotype Optic Atrophy, Hereditary, Leber Usher Syndromes Mutation, Missense Macular Degeneration Retinal Cone Photoreceptor Cells Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Codon, Nonsense Exons Optic Disk Drusen Sarcoglycans Kidney Diseases, Cystic Lipofuscin Rats, Mutant Strains Visual Fields Heteroduplex Analysis Genetic Linkage Tomography, Optical Coherence Rhodopsin Exome Molecular Sequence Data Muscular Dystrophy, Oculopharyngeal Visual Field Tests Dystroglycans Chromosome Mapping Reflex Sympathetic Dystrophy Homozygote Age of Onset Heterozygote Vision Disorders Polymorphism, Single-Stranded Conformational Lod Score Frameshift Mutation Abnormalities, Multiple Ophthalmoscopy Nerve Tissue Proteins Utrophin Muscle, Skeletal Vitelliform Macular Dystrophy Intermediate Filament Proteins Haplotypes Base Sequence Genetic Testing Intellectual Disability Carrier Proteins Rod Opsins Membrane Proteins Genotype Rod Cell Outer Segment Proteins ATP-Binding Cassette Transporters Disease Models, Animal Guanylate Cyclase Polymerase Chain Reaction Amino Acid Sequence

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