Human retinal diseases genes cases retinal dystrophies. Medical search. Frequent questions

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Anatomy12

Retina Fundus Oculi Photoreceptor Cells, Vertebrate Retinal Pigment Epithelium Pigment Epithelium of Eye Retinal Rod Photoreceptor Cells Photoreceptor Cells Retinal Cone Photoreceptor Cells Retinal Vessels Rod Cell Outer Segment Ependymoglial Cells Chromosomes, Human, Pair 4

Organisms3

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

Diseases41

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

Chemicals and Drugs18

Eye Proteins cis-trans-Isomerases Peripherins Lipofuscin Dystrophin Rhodopsin Cyclic Nucleotide Phosphodiesterases, Type 6 Nerve Tissue Proteins Rod Opsins Intermediate Filament Proteins Codon, Nonsense Genetic Markers Carrier Proteins Sarcoglycans ATP-Binding Cassette Transporters Proteins Membrane Proteins Dystroglycans

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

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

Psychiatry and Psychology4

Visual Acuity Vision, Ocular Visual Fields Intellectual Disability

Phenomena and Processes29

Genes, Recessive Mutation Consanguinity Genetic Linkage Phenotype Genes, Dominant Dark Adaptation Visual Acuity Mutation, Missense Exons Lod Score Exome Vision, Ocular Visual Fields Haplotypes Polymorphism, Single-Stranded Conformational Codon, Nonsense Base Sequence Genotype Homozygote Genetic Markers Heterozygote Amino Acid Sequence Frameshift Mutation Chromosomes, Human, Pair 4 Genetic Predisposition to Disease Light Polymorphism, Single Nucleotide Genome, Human

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Databases, Genetic

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 Diseases Retinal Degeneration Retinal Dystrophies Muscular Dystrophies Leber Congenital Amaurosis Retinitis Pigmentosa Myotonic Dystrophy Electroretinography Eye Proteins cis-trans-Isomerases Muscular Dystrophy, Duchenne Retina Fundus Oculi Pedigree Photoreceptor Cells, Vertebrate Corneal Dystrophies, Hereditary Eye Diseases, Hereditary Genes, Recessive Muscular Dystrophy, Animal Retinal Pigment Epithelium Peripherins Pigment Epithelium of Eye Mutation Consanguinity Night Blindness Genetic Diseases, Inborn Blindness DNA Mutational Analysis Retinal Rod Photoreceptor Cells Fuchs' Endothelial Dystrophy Lipofuscin Laurence-Moon Syndrome Genetic Linkage Photoreceptor Cells Macular Degeneration Chromosome Mapping Retinal Cone Photoreceptor Cells Disease Phenotype Genes, Dominant Usher Syndromes Dark Adaptation Visual Acuity Fluorescein Angiography Muscular Dystrophy, Facioscapulohumeral Dystrophin Tomography, Optical Coherence Rhodopsin Mutation, Missense Bardet-Biedl Syndrome Ophthalmoscopy Microphthalmos Exons Lod Score Molecular Sequence Data Cyclic Nucleotide Phosphodiesterases, Type 6 Exome Alstrom Syndrome Vision, Ocular Visual Fields Syndrome Nerve Tissue Proteins Visual Field Tests Haplotypes Muscular Dystrophy, Emery-Dreifuss Kidney Diseases, Cystic Mice, Inbred mdx Polymorphism, Single-Stranded Conformational Vision Disorders Rod Opsins Intermediate Filament Proteins Retinal Vessels Codon, Nonsense Optic Atrophy, Hereditary, Leber Base Sequence Disease Models, Animal Genotype Homozygote Ophthalmoscopes Genetic Markers Genetic Testing Choroid Diseases Neuroaxonal Dystrophies Optic Atrophies, Hereditary Carrier Proteins Heterozygote Optic Disk Drusen Sarcoglycans ATP-Binding Cassette Transporters Age of Onset Rats, Mutant Strains Amino Acid Sequence Rod Cell Outer Segment Proteins Frameshift Mutation Heteroduplex Analysis Intellectual Disability Abnormalities, Multiple Mice, Inbred C57BL Membrane Proteins

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