Amaurosis retinal dystrophies. Medical search. Frequent questions

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Anatomy12

Fundus Oculi Photoreceptor Cells, Vertebrate Retina Pigment Epithelium of Eye Retinal Rod Photoreceptor Cells Retinal Cone Photoreceptor Cells Photoreceptor Cells Retinal Pigment Epithelium Photoreceptor Connecting Cilium Muscle, Skeletal Rod Cell Outer Segment Carotid Artery, Internal

Organisms5

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

Diseases43

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

Chemicals and Drugs23

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment18

Electroretinography Pedigree DNA Mutational Analysis Visual Acuity Fluorescein Angiography Tomography, Optical Coherence Visual Field Tests Chromosome Mapping Heteroduplex Analysis Genetic Testing Disease Models, Animal Ophthalmoscopy Genetic Therapy Polymerase Chain Reaction Injections, Intraocular Sequence Analysis, DNA Reflex, Pupillary Endarterectomy, Carotid

Psychiatry and Psychology5

Visual Acuity Visual Fields Vision, Ocular Night Vision Intellectual Disability

Phenomena and Processes31

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

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Genetic Testing Age of Onset

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

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