Retinitis pigmentosa retinal diseases. Medical search. Frequent questions

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Anatomy21

Photoreceptor Cells, Vertebrate Retina Fundus Oculi Retinal Rod Photoreceptor Cells Photoreceptor Cells Retinal Cone Photoreceptor Cells Retinal Pigment Epithelium X Chromosome Pigment Epithelium of Eye Fovea Centralis Macula Lutea Retinal Photoreceptor Cell Outer Segment Photoreceptor Connecting Cilium Retinal Vessels Rod Cell Outer Segment Cilia Choroid Retinal Neurons Vitreous Body Retinal Ganglion Cells Retinal Bipolar Cells

Organisms3

Dependovirus Mice, Inbred C57BL Rats, Transgenic

Diseases27

Retinitis Pigmentosa Retinal Diseases Cytomegalovirus Retinitis Retinal Degeneration Retinitis Genetic Diseases, X-Linked Night Blindness Usher Syndromes Leber Congenital Amaurosis Blindness Eye Diseases, Hereditary Retinal Dystrophies Vision Disorders Eye Infections, Viral Macular Degeneration Disease Models, Animal Laurence-Moon Syndrome Vision, Low Retinal Dysplasia Optic Atrophy, Hereditary, Leber Ataxia Color Vision Defects Bardet-Biedl Syndrome Syndrome Dog Diseases Optic Atrophies, Hereditary Eye Diseases

Chemicals and Drugs20

Eye Proteins Rhodopsin Peripherins Cyclic Nucleotide Phosphodiesterases, Type 6 Rod Opsins cis-trans-Isomerases Intermediate Filament Proteins IMP Dehydrogenase Carbonic Anhydrase IV Ribonucleoprotein, U4-U6 Small Nuclear Tetraspanins Opsins Lipofuscin Retinaldehyde Carrier Proteins Codon, Nonsense Nerve Tissue Proteins Foscarnet Membrane Proteins Arrestin

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

Electroretinography Pedigree Visual Acuity DNA Mutational Analysis Visual Field Tests Tomography, Optical Coherence Fluorescein Angiography Ophthalmoscopes Ophthalmoscopy Disease Models, Animal Chromosome Mapping Visual Prosthesis Fluorescent Antibody Technique, Indirect Polymerase Chain Reaction Sequence Analysis, DNA Vision Tests Genetic Therapy Electrooculography Diagnostic Techniques, Ophthalmological

Psychiatry and Psychology5

Visual Acuity Visual Fields Vision, Ocular Sensory Thresholds Phosphenes

Phenomena and Processes27

Genes, Dominant Genes, Recessive Dark Adaptation Visual Acuity Visual Fields Mutation Genetic Linkage Consanguinity X Chromosome Exons Mutation, Missense Vision, Ocular Polymorphism, Single-Stranded Conformational Homozygote Phenotype Lod Score Amino Acid Sequence Base Sequence Light Frameshift Mutation Genes, X-Linked Phosphenes Heterozygote Codon, Nonsense Genotype Point Mutation RNA Splicing

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

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

Retinitis Pigmentosa Retinal Diseases Electroretinography Cytomegalovirus Retinitis Eye Proteins Retinal Degeneration Rhodopsin Photoreceptor Cells, Vertebrate Retinitis Retina Genes, Dominant Pedigree Peripherins Fundus Oculi Genes, Recessive Cyclic Nucleotide Phosphodiesterases, Type 6 Retinal Rod Photoreceptor Cells Dark Adaptation Genetic Diseases, X-Linked Photoreceptor Cells Visual Acuity Retinal Cone Photoreceptor Cells Night Blindness Usher Syndromes Visual Fields Mutation Leber Congenital Amaurosis DNA Mutational Analysis Blindness Eye Diseases, Hereditary Rod Opsins Genetic Linkage Visual Field Tests Retinal Pigment Epithelium Tomography, Optical Coherence Fluorescein Angiography Consanguinity cis-trans-Isomerases X Chromosome Pigment Epithelium of Eye Exons Mutation, Missense Retinal Dystrophies Fovea Centralis Vision, Ocular Ophthalmoscopes Molecular Sequence Data Intermediate Filament Proteins Vision Disorders Ophthalmoscopy Eye Infections, Viral Macular Degeneration Polymorphism, Single-Stranded Conformational IMP Dehydrogenase Homozygote Phenotype Disease Models, Animal Laurence-Moon Syndrome Macula Lutea Chromosome Mapping Carbonic Anhydrase IV Visual Prosthesis Ribonucleoprotein, U4-U6 Small Nuclear Retinal Photoreceptor Cell Outer Segment Tetraspanins Lod Score Photoreceptor Connecting Cilium Vision, Low Retinal Vessels Amino Acid Sequence Sensory Thresholds Opsins Base Sequence Lipofuscin Light Frameshift Mutation Genes, X-Linked Rod Cell Outer Segment Retinal Dysplasia Dependovirus Fluorescent Antibody Technique, Indirect Optic Atrophy, Hereditary, Leber Ataxia Phosphenes Polymerase Chain Reaction Heterozygote Sequence Analysis, DNA Retinaldehyde Carrier Proteins Codon, Nonsense Vision Tests Color Vision Defects Bardet-Biedl Syndrome Genotype Syndrome Genetic Therapy Cilia Nerve Tissue Proteins Point Mutation Mice, Inbred C57BL

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