Macular or cone retinal dystrophies. Medical search. Frequent questions

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Anatomy12

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

Organisms4

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

Diseases38

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

Chemicals and Drugs24

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Heteroduplex Analysis Tomography, Optical Coherence Ophthalmoscopy Visual Field Tests Chromosome Mapping Genetic Testing Disease Models, Animal Polymerase Chain Reaction Cone-Beam Computed Tomography Sequence Analysis, DNA Amino Acid Substitution

Psychiatry and Psychology4

Visual Acuity Visual Fields Vision, Ocular Intellectual Disability

Phenomena and Processes28

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

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

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